run_metadata
2,219 rows where experiment.library_layout = "PAIRED", experiment.library_source = "TRANSCRIPTOMIC" and tissue_curation = "Trunk"
This data as json, CSV (advanced)
| Link | rowid ▼ | run.accession | experiment.accession | sample.accession | study.accession | bioproject | study.title | study.alias | study.type | study.abstract | study.attributes | study.PMIDs | sample.description | sample.title | sample.alias | sample.centername | sample.attributes | GEOsample.title | GEOsample.dataprocessing | GEOsample.source | GEOsample.treatmentprotocol | GEOsample.extractprotocol | GEOsample.growthprotocol | GEOsample.characteristics | GEOsample.accession | experiment.title | experiment.alias | experiment.library_name | experiment.design_description | experiment.library_construction_protocol | experiment.attributes | experiment.library_strategy | experiment.library_source | experiment.library_selection | experiment.library_layout | experiment.platform | experiment.instrument_model | experiment.spot_descriptor | experiment.study_ref | run.title | run.attributes | run.filename | run.semantic_name | run.total_bases | run.total_spots | run.alias | run.read_lengths | run.base_counts | run.r1_length | run.r2_length | run.r3_length | run.r4_length | run.Acount | run.Ccount | run.Gcount | run.Tcount | run.Ncount | run.experiment | run.pool_member | submission.accession | submission.srasource | submission.bioprojectsource | seqdetective.n_mates | seqdetective.mapping_rate.mate1 | seqdetective.mapping_rate.mate2 | seqdetective.nofeature_rate.mate1 | seqdetective.nofeature_rate.mate2 | seqdetective.sparsity.mate1 | seqdetective.sparsity.mate2 | seqdetective.pos_strand_rate.mate1 | seqdetective.pos_strand_rate.mate2 | seqdetective.readlen.mate1 | seqdetective.readlen.mate2 | seqdetective.judgement.mate1 | seqdetective.judgement.mate2 | seqdetective.judgement.reason | platform_family | instrument_generation | read_bias | selection_class | prep_kit | sc_or_bulk | tech_class | technology | tech_variant | submission.bioprojectsource.country | earliest_date | devstage_curation | devstage_curation_coarse | tissue_curation | tissue_curation_coarse |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 9170 | 9170 | ERR216332 | ERX190997 | ERS094086 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689285 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:male|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T17:02:18Z|ENA LAST UPDATE:2018 03 08T15:36:37Z|External Id:SAMEA1689285|INSDC center name:SC|INSDC first public:2013 01 07T17:02:18Z|INSDC last update:2018 03 08T15:36:37Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:29Z 1355130|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:29Z 1355130|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#6 | 4927108 | Illumina sequencing of library 4927108 constructed from sample accession ERS094086 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence GCCAATGT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#6.bam | bam | 3849223200.0 | 25661488.0 | SC RUN 7896 6#6 | 0:75 1:75 | A:1052343872;C:867977827;G:867966925;T:1060514703;N:419873 | 75 | 75 | 1052343872 | 867977827 | 867966925 | 1060514703 | 419873 | ERX190997 | ERS094086 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.94843 | 0.9504 | 0.09374 | 0.09366 | 0.71421 | 0.71916 | 0.5306 | 0.52809 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 9171 | 9171 | ERR216331 | ERX190996 | ERS094085 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689286 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:male|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T17:02:18Z|ENA LAST UPDATE:2018 03 08T15:36:15Z|External Id:SAMEA1689286|INSDC center name:SC|INSDC first public:2013 01 07T17:02:18Z|INSDC last update:2018 03 08T15:36:15Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:28Z 1355129|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:28Z 1355129|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#5 | 4927107 | Illumina sequencing of library 4927107 constructed from sample accession ERS094085 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence ACAGTGGT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#5.bam | bam | 5957027700.0 | 39713518.0 | SC RUN 7896 6#5 | 0:75 1:75 | A:1634176455;C:1344899134;G:1345048404;T:1632256963;N:646744 | 75 | 75 | 1634176455 | 1344899134 | 1345048404 | 1632256963 | 646744 | ERX190996 | ERS094085 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.94169 | 0.94387 | 0.09489 | 0.09587 | 0.69406 | 0.69869 | 0.51459 | 0.51918 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 9172 | 9172 | ERR216330 | ERX190995 | ERS094084 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689283 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:male|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T17:02:18Z|ENA LAST UPDATE:2018 03 08T15:36:37Z|External Id:SAMEA1689283|INSDC center name:SC|INSDC first public:2013 01 07T17:02:18Z|INSDC last update:2018 03 08T15:36:37Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:28Z 1355128|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:28Z 1355128|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#4 | 4927106 | Illumina sequencing of library 4927106 constructed from sample accession ERS094084 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence TGACCACT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#4.bam | bam | 4130918700.0 | 27539458.0 | SC RUN 7896 6#4 | 0:75 1:75 | A:1129107864;C:933544249;G:934913323;T:1132901907;N:451357 | 75 | 75 | 1129107864 | 933544249 | 934913323 | 1132901907 | 451357 | ERX190995 | ERS094084 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.94225 | 0.94433 | 0.09272 | 0.09299 | 0.70043 | 0.70534 | 0.51333 | 0.52182 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 9173 | 9173 | ERR216329 | ERX190994 | ERS094083 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689282 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:female|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T17:02:18Z|ENA LAST UPDATE:2018 03 08T15:36:37Z|External Id:SAMEA1689282|INSDC center name:SC|INSDC first public:2013 01 07T17:02:18Z|INSDC last update:2018 03 08T15:36:37Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:27Z 1355127|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:27Z 1355127|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#3 | 4927105 | Illumina sequencing of library 4927105 constructed from sample accession ERS094083 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence TTAGGCAT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#3.bam | bam | 5102725800.0 | 34018172.0 | SC RUN 7896 6#3 | 0:75 1:75 | A:1400946711;C:1145033579;G:1143298888;T:1412890130;N:556492 | 75 | 75 | 1400946711 | 1145033579 | 1143298888 | 1412890130 | 556492 | ERX190994 | ERS094083 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.93688 | 0.93952 | 0.07363 | 0.07321 | 0.69645 | 0.70161 | 0.48708 | 0.48926 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 9174 | 9174 | ERR216328 | ERX190993 | ERS094082 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689281 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:female|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T10:04:12Z|ENA LAST UPDATE:2018 03 08T15:36:11Z|External Id:SAMEA1689281|INSDC center name:SC|INSDC first public:2013 01 07T10:04:12Z|INSDC last update:2018 03 08T15:36:11Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:26Z 1355126|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:26Z 1355126|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#2 | 4927104 | Illumina sequencing of library 4927104 constructed from sample accession ERS094082 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence CGATGTTT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#2.bam | bam | 4350577950.0 | 29003853.0 | SC RUN 7896 6#2 | 0:75 1:75 | A:1214100125;C:955724962;G:954429461;T:1225838270;N:485132 | 75 | 75 | 1214100125 | 955724962 | 954429461 | 1225838270 | 485132 | ERX190993 | ERS094082 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.92911 | 0.93026 | 0.0749 | 0.07514 | 0.69418 | 0.69775 | 0.48934 | 0.49 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 9175 | 9175 | ERR216327 | ERX190992 | ERS094081 | ERP001234 | PRJEB2894 | ZF adult transcriptome | ZF_adult_transcriptome-sc-2012-02-20T14:37:57Z-2125 | Transcriptome Analysis | Paired end sequence data from the Illumina HiSeq was prepared from male and female adult zebrafish for transcript ome analysis. | SAMEA1689284 | SC | ArrayExpress DevelopmentalStage:Adult|ArrayExpress OrganismPart:Whole body|ArrayExpress Sex:male|ArrayExpress Species:Danio rerio|ENA FIRST PUBLIC:2013 01 07T17:02:18Z|ENA LAST UPDATE:2018 03 08T15:36:37Z|External Id:SAMEA1689284|INSDC center name:SC|INSDC first public:2013 01 07T17:02:18Z|INSDC last update:2018 03 08T15:36:37Z|INSDC status:public|Submitter Id:Adult zebrafish body sc 2012 02 09T16:35:23Z 1355125|common name:zebrafish|sample description:Total RNA from zebrafish body|sample name:Adult zebrafish body sc 2012 02 09T16:35:23Z 1355125|scientific name:Danio rerio|strain:SAT | 1 | SC EXP 7896 6#1 | 4927103 | Illumina sequencing of library 4927103 constructed from sample accession ERS094081 for study accession ERP001234. This is part of an Illumina multiplexed sequencing run 7896 6. This submission includes reads tagged with the sequence ATCACGTT. | Illumina cDNA protocol | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | ERP001234 | Illumina HiSeq 2000 paired end sequencing | ENA FIRST PUBLIC:2013 01 07|ENA LAST UPDATE:2018 11 16 | 7896_6#1.bam | bam | 5063629350.0 | 33757529.0 | SC RUN 7896 6#1 | 0:75 1:75 | A:1416301768;C:1110273098;G:1105481234;T:1431015934;N:557316 | 75 | 75 | 1416301768 | 1110273098 | 1105481234 | 1431015934 | 557316 | ERX190992 | ERS094081 | ERA182034 | SC | Wellcome Sanger Institute | 2 | 0.93508 | 0.93634 | 0.11212 | 0.11206 | 0.70009 | 0.70538 | 0.50126 | 0.49177 | 75 | 75 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | United Kingdom | 2013-01-07 | Adult | Adult | Trunk | Surface Structure | |||||||||||||||||
| 11148 | 11148 | ERR10034072 | ERX9574476 | ERS12562187 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Metamorphic tissue without xxx from Danio rerio | Drerio metamorphic 5 | SAMEA110464159 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464159|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE25|collected by:Marco Podobnik|collection date:2018 06 27|common name:zebrafish|dev stage:Metamorphic|identified by:Marco Podobnik|sample name:SAMPLE25|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:835 19178 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr25.1.fastq.gz S879Nr25.2.fastq.gz | fastq fastq | 10120435126.0 | 50403985.0 | ena RUN TAB 05 08 2022 14:25:08:835 19179 | 0:100.39 1:100.39 | A:2679131890;C:2420708190;G:2483153503;T:2537307238;N:134305 | 100 | 100 | 2679131890 | 2420708190 | 2483153503 | 2537307238 | 134305 | ERX9574476 | ERS12562187 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.96973 | 0.97106 | 0.04979 | 0.04949 | 0.71252 | 0.71654 | 0.4806 | 0.49338 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Undetermined | Undetermined | Trunk | Surface Structure | ||||||||||||||
| 11149 | 11149 | ERR10034071 | ERX9574475 | ERS12562186 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Metamorphic tissue without xxx from Danio rerio | Drerio metamorphic 4 | SAMEA110464158 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464158|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE24|collected by:Marco Podobnik|collection date:2018 06 27|common name:zebrafish|dev stage:Metamorphic|identified by:Marco Podobnik|sample name:SAMPLE24|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:835 19176 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr24.1.fastq.gz S879Nr24.2.fastq.gz | fastq fastq | 7845661906.0 | 39121993.0 | ena RUN TAB 05 08 2022 14:25:08:835 19177 | 0:100.27 1:100.27 | A:2096079479;C:1862247618;G:1929220494;T:1958006859;N:107456 | 100 | 100 | 2096079479 | 1862247618 | 1929220494 | 1958006859 | 107456 | ERX9574475 | ERS12562186 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.96989 | 0.96986 | 0.04901 | 0.04902 | 0.71599 | 0.72301 | 0.48965 | 0.48827 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Undetermined | Undetermined | Trunk | Surface Structure | ||||||||||||||
| 11150 | 11150 | ERR10034070 | ERX9574474 | ERS12562185 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Metamorphic tissue without xxx from Danio rerio | Drerio metamorphic 3 | SAMEA110464157 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464157|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE23|collected by:Marco Podobnik|collection date:2018 06 27|common name:zebrafish|dev stage:Metamorphic|identified by:Marco Podobnik|sample name:SAMPLE23|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:835 19174 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr23.1.fastq.gz S879Nr23.2.fastq.gz | fastq fastq | 8270390422.0 | 41338131.0 | ena RUN TAB 05 08 2022 14:25:08:835 19175 | 0:100.03 1:100.03 | A:2156060704;C:1998612686;G:2055201244;T:2060404840;N:110948 | 100 | 100 | 2156060704 | 1998612686 | 2055201244 | 2060404840 | 110948 | ERX9574474 | ERS12562185 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.97085 | 0.97083 | 0.04232 | 0.04236 | 0.7219 | 0.72671 | 0.47325 | 0.4807 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Undetermined | Undetermined | Trunk | Surface Structure | ||||||||||||||
| 11151 | 11151 | ERR10034069 | ERX9574473 | ERS12562184 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Metamorphic tissue without xxx from Danio rerio | Drerio metamorphic 2 | SAMEA110464156 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464156|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE22|collected by:Marco Podobnik|collection date:2018 06 27|common name:zebrafish|dev stage:Metamorphic|identified by:Marco Podobnik|sample name:SAMPLE22|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:834 19172 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr22.1.fastq.gz S879Nr22.2.fastq.gz | fastq fastq | 10977356920.0 | 54380062.0 | ena RUN TAB 05 08 2022 14:25:08:834 19173 | 0:100.93 1:100.93 | A:2852856166;C:2671616791;G:2798184312;T:2654546853;N:152798 | 100 | 100 | 2852856166 | 2671616791 | 2798184312 | 2654546853 | 152798 | ERX9574473 | ERS12562184 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.9765 | 0.97629 | 0.03531 | 0.03529 | 0.72025 | 0.72705 | 0.47808 | 0.46326 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Undetermined | Undetermined | Trunk | Surface Structure | ||||||||||||||
| 11152 | 11152 | ERR10034068 | ERX9574472 | ERS12562183 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Metamorphic tissue without xxx from Danio rerio | Drerio metamorphic 1 | SAMEA110464155 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464155|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE21|collected by:Marco Podobnik|collection date:2018 06 27|common name:zebrafish|dev stage:Metamorphic|identified by:Marco Podobnik|sample name:SAMPLE21|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:834 19170 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr21.1.fastq.gz S879Nr21.2.fastq.gz | fastq fastq | 11346084502.0 | 56210802.0 | ena RUN TAB 05 08 2022 14:25:08:834 19171 | 0:100.92 1:100.92 | A:2950787998;C:2755514202;G:2902131288;T:2737495846;N:155168 | 100 | 100 | 2950787998 | 2755514202 | 2902131288 | 2737495846 | 155168 | ERX9574472 | ERS12562183 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.9732 | 0.97208 | 0.02959 | 0.02983 | 0.72322 | 0.73135 | 0.47796 | 0.47326 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Undetermined | Undetermined | Trunk | Surface Structure | ||||||||||||||
| 11153 | 11153 | ERR10034052 | ERX9574456 | ERS12562167 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Larval tissue without xxx from Danio rerio | Drerio larval 5 | SAMEA110464139 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464139|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE5|collected by:Marco Podobnik|collection date:2018 06 19|common name:zebrafish|dev stage:Larval|identified by:Marco Podobnik|sample name:SAMPLE5|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:829 19138 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr5.1.fastq.gz S879Nr5.2.fastq.gz | fastq fastq | 7308445864.0 | 36509997.0 | ena RUN TAB 05 08 2022 14:25:08:829 19139 | 0:100.09 1:100.09 | A:1934019972;C:1742739870;G:1803466955;T:1828120200;N:98867 | 100 | 100 | 1934019972 | 1742739870 | 1803466955 | 1828120200 | 98867 | ERX9574456 | ERS12562167 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.96596 | 0.96653 | 0.05312 | 0.05284 | 0.71323 | 0.71873 | 0.49632 | 0.48138 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Larval | Larval | Trunk | Surface Structure | ||||||||||||||
| 11154 | 11154 | ERR10034051 | ERX9574455 | ERS12562166 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Larval tissue without xxx from Danio rerio | Drerio larval 4 | SAMEA110464138 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464138|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE4|collected by:Marco Podobnik|collection date:2018 06 19|common name:zebrafish|dev stage:Larval|identified by:Marco Podobnik|sample name:SAMPLE4|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:822 19136 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr4.1.fastq.gz S879Nr4.2.fastq.gz | fastq fastq | 8046902370.0 | 40206331.0 | ena RUN TAB 05 08 2022 14:25:08:829 19137 | 0:100.07 1:100.07 | A:2154247315;C:1901540683;G:1965167700;T:2025838764;N:107908 | 100 | 100 | 2154247315 | 1901540683 | 1965167700 | 2025838764 | 107908 | ERX9574455 | ERS12562166 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.96507 | 0.96543 | 0.05345 | 0.0533 | 0.71553 | 0.72123 | 0.48553 | 0.49 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Larval | Larval | Trunk | Surface Structure | ||||||||||||||
| 11155 | 11155 | ERR10034050 | ERX9574454 | ERS12562165 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Larval tissue without xxx from Danio rerio | Drerio larval 3 | SAMEA110464137 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464137|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE3|collected by:Marco Podobnik|collection date:2018 06 19|common name:zebrafish|dev stage:Larval|identified by:Marco Podobnik|sample name:SAMPLE3|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:821 19134 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr3.1.fastq.gz S879Nr3.2.fastq.gz | fastq fastq | 10897526786.0 | 54442757.0 | ena RUN TAB 05 08 2022 14:25:08:821 19135 | 0:100.08 1:100.08 | A:2902340346;C:2590905706;G:2655361716;T:2748771201;N:147817 | 100 | 100 | 2902340346 | 2590905706 | 2655361716 | 2748771201 | 147817 | ERX9574454 | ERS12562165 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.93244 | 0.93322 | 0.04311 | 0.04269 | 0.72452 | 0.72723 | 0.49726 | 0.4784 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Larval | Larval | Trunk | Surface Structure | ||||||||||||||
| 11156 | 11156 | ERR10034049 | ERX9574453 | ERS12562164 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Larval tissue without xxx from Danio rerio | Drerio larval 2 | SAMEA110464136 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464136|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE2|collected by:Marco Podobnik|collection date:2018 06 19|common name:zebrafish|dev stage:Larval|identified by:Marco Podobnik|sample name:SAMPLE2|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:821 19132 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr2.1.fastq.gz S879Nr2.2.fastq.gz | fastq fastq | 8516273680.0 | 42589650.0 | ena RUN TAB 05 08 2022 14:25:08:821 19133 | 0:99.98 1:99.98 | A:2232300748;C:2055212367;G:2121115843;T:2107529926;N:114796 | 99 | 99 | 2232300748 | 2055212367 | 2121115843 | 2107529926 | 114796 | ERX9574453 | ERS12562164 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.97117 | 0.97187 | 0.05876 | 0.05804 | 0.72115 | 0.72689 | 0.51447 | 0.50827 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Larval | Larval | Trunk | Surface Structure | ||||||||||||||
| 11157 | 11157 | ERR10034048 | ERX9574452 | ERS12562163 | ERP140005 | PRJEB55122 | Danio developmental transcriptomes | ca4a518e-aaf7-42d9-9758-352aac808809 | Other | Transcriptomic analysis of four different developmental stages of four Danio species D. rerio D. aesculapii Danio aff. kyathit striped also known as Danio quagga and D. albolineatus. Five biological replicates were sampled for every developmental stage of a species. | ENA FIRST PUBLIC:2022 08 05|ENA LAST UPDATE:2022 08 08 | Larval tissue without xxx from Danio rerio | Drerio larval 1 | SAMEA110464135 | max planck institute for biology | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08|External Id:SAMEA110464135|INSDC center alias:MAX PLANCK INSTITUTE FOR BIOLOGY|INSDC center name:max planck institute for biology|INSDC first public:2022 08 08T04:26:46Z|INSDC last update:2022 08 08T04:26:46Z|INSDC status:public|Submitter Id:SAMPLE1|collected by:Marco Podobnik|collection date:2018 06 19|common name:zebrafish|dev stage:Larval|identified by:Marco Podobnik|sample name:SAMPLE1|sex:not provided|tissue type:whole body without xxx | Illumina NovaSeq 6000 paired end sequencing | ena EXPERIMENT TAB 05 08 2022 14:25:08:820 19130 | unspecified | 1 | Illumina TruSeq DNA Nano Kit | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | ERP140005 | Illumina NovaSeq 6000 paired end sequencing | ENA FIRST PUBLIC:2022 08 08|ENA LAST UPDATE:2022 08 08 | S879Nr1.1.fastq.gz S879Nr1.2.fastq.gz | fastq fastq | 5477863098.0 | 27332001.0 | ena RUN TAB 05 08 2022 14:25:08:821 19131 | 0:100.21 1:100.21 | A:1436230762;C:1320194529;G:1370010454;T:1351352868;N:74485 | 100 | 100 | 1436230762 | 1320194529 | 1370010454 | 1351352868 | 74485 | ERX9574452 | ERS12562163 | ERA16814395 | max planck institute for biology|European Nucleotide Archive | max planck institute for biology | 2 | 0.97196 | 0.97163 | 0.05932 | 0.05814 | 0.72723 | 0.73348 | 0.50582 | 0.51053 | 101 | 101 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2022-08-05 | Larval | Larval | Trunk | Surface Structure | ||||||||||||||
| 24600 | 24600 | SRR25475196 | SRX21207464 | SRS18464933 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/50 [PrP BMD5 50 3] | GSM7671235 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/50 [PrP BMD5 50 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50 | GSM7671235 | GSM7671235: Zebrafish PrP BMD5/50 [PrP BMD5 50 3]; Danio rerio; RNA Seq | GSM7671235 r1 | GSM7671235 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_50_3_1.fq.gz PrP_BMD5_50_3_2.fq.gz | fastq fastq | 5877585306.0 | 19462203.0 | GSM7671235 r1 | 0:151 1:151 | A:1673096549;C:1287336870;G:1399452621;T:1517513965;N:185301 | 151 | 151 | 1673096549 | 1287336870 | 1399452621 | 1517513965 | 185301 | SRX21207464 | SRS18464933 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94721 | 0.94392 | 0.10307 | 0.10285 | 0.71474 | 0.7209 | 0.44676 | 0.44767 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24601 | 24601 | SRR25475197 | SRX21207464 | SRS18464933 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/50 [PrP BMD5 50 3] | GSM7671235 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/50 [PrP BMD5 50 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50 | GSM7671235 | GSM7671235: Zebrafish PrP BMD5/50 [PrP BMD5 50 3]; Danio rerio; RNA Seq | GSM7671235 r1 | GSM7671235 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_50_3_3.fq.gz PrP_BMD5_50_3_4.fq.gz | fastq fastq | 2592008620.0 | 8582810.0 | GSM7671235 r2 | 0:151 1:151 | A:736893507;C:572181175;G:612346091;T:670582360;N:5487 | 151 | 151 | 736893507 | 572181175 | 612346091 | 670582360 | 5487 | SRX21207464 | SRS18464933 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94766 | 0.94372 | 0.10432 | 0.10439 | 0.71108 | 0.7193 | 0.4466 | 0.45067 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24602 | 24602 | SRR25475198 | SRX21207463 | SRS18464932 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/50 [PrP BMD5 50 2] | GSM7671234 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/50 [PrP BMD5 50 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50 | GSM7671234 | GSM7671234: Zebrafish PrP BMD5/50 [PrP BMD5 50 2]; Danio rerio; RNA Seq | GSM7671234 r1 | GSM7671234 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_50_2_1.fq.gz PrP_BMD5_50_2_2.fq.gz | fastq fastq | 6523053228.0 | 21599514.0 | GSM7671234 r1 | 0:151 1:151 | A:1881747155;C:1402382759;G:1625853412;T:1612862952;N:206950 | 151 | 151 | 1881747155 | 1402382759 | 1625853412 | 1612862952 | 206950 | SRX21207463 | SRS18464932 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94694 | 0.93482 | 0.08725 | 0.08666 | 0.70729 | 0.72423 | 0.44992 | 0.43992 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24603 | 24603 | SRR25475199 | SRX21207462 | SRS18464931 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/50 [PrP BMD5 50 1] | GSM7671233 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/50 [PrP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50 | GSM7671233 | GSM7671233: Zebrafish PrP BMD5/50 [PrP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671233 r1 | GSM7671233 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_50_1_1.fq.gz PrP_BMD5_50_1_2.fq.gz | fastq fastq | 2090436450.0 | 6921975.0 | GSM7671233 r1 | 0:151 1:151 | A:595082772;C:455110337;G:489835116;T:550342388;N:65837 | 151 | 151 | 595082772 | 455110337 | 489835116 | 550342388 | 65837 | SRX21207462 | SRS18464931 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.93897 | 0.93808 | 0.1192 | 0.11852 | 0.71703 | 0.71938 | 0.46566 | 0.48323 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24604 | 24604 | SRR25475200 | SRX21207462 | SRS18464931 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/50 [PrP BMD5 50 1] | GSM7671233 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/50 [PrP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/50 | GSM7671233 | GSM7671233: Zebrafish PrP BMD5/50 [PrP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671233 r1 | GSM7671233 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_50_1_3.fq.gz PrP_BMD5_50_1_4.fq.gz | fastq fastq | 4126091912.0 | 13662556.0 | GSM7671233 r2 | 0:151 1:151 | A:1171476389;C:902866887;G:958669795;T:1093069759;N:9082 | 151 | 151 | 1171476389 | 902866887 | 958669795 | 1093069759 | 9082 | SRX21207462 | SRS18464931 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.93709 | 0.93594 | 0.1203 | 0.11941 | 0.71666 | 0.71924 | 0.47229 | 0.47483 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24605 | 24605 | SRR25475201 | SRX21207461 | SRS18464930 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/10 [PrP BMD5 10 3] | GSM7671232 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/10 [PrP BMD5 10 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10 | GSM7671232 | GSM7671232: Zebrafish PrP BMD5/10 [PrP BMD5 10 3]; Danio rerio; RNA Seq | GSM7671232 r1 | GSM7671232 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_10_3_1.fq.gz PrP_BMD5_10_3_2.fq.gz | fastq fastq | 6850831646.0 | 22684873.0 | GSM7671232 r1 | 0:151 1:151 | A:1937014178;C:1514493141;G:1623449869;T:1775656465;N:217993 | 151 | 151 | 1937014178 | 1514493141 | 1623449869 | 1775656465 | 217993 | SRX21207461 | SRS18464930 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94857 | 0.94727 | 0.09818 | 0.0981 | 0.70849 | 0.71364 | 0.44643 | 0.44849 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24606 | 24606 | SRR25475202 | SRX21207460 | SRS18464929 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/10 [PrP BMD5 10 2] | GSM7671231 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/10 [PrP BMD5 10 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10 | GSM7671231 | GSM7671231: Zebrafish PrP BMD5/10 [PrP BMD5 10 2]; Danio rerio; RNA Seq | GSM7671231 r1 | GSM7671231 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_10_2_2.fq.gz PrP_BMD5_10_2_1.fq.gz | fastq fastq | 6143720390.0 | 20343445.0 | GSM7671231 r1 | 0:151 1:151 | A:1724246127;C:1362285676;G:1457061100;T:1599935999;N:191488 | 151 | 151 | 1724246127 | 1362285676 | 1457061100 | 1599935999 | 191488 | SRX21207460 | SRS18464929 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9488 | 0.94766 | 0.094 | 0.09263 | 0.70905 | 0.71348 | 0.45157 | 0.43474 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24607 | 24607 | SRR25475203 | SRX21207459 | SRS18464928 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/10 [PrP BMD5 10 1] | GSM7671230 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/10 [PrP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10 | GSM7671230 | GSM7671230: Zebrafish PrP BMD5/10 [PrP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671230 r1 | GSM7671230 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_10_1_1.fq.gz PrP_BMD5_10_1_2.fq.gz | fastq fastq | 4178827454.0 | 13837177.0 | GSM7671230 r1 | 0:151 1:151 | A:1203579431;C:904927450;G:969023531;T:1101165327;N:131715 | 151 | 151 | 1203579431 | 904927450 | 969023531 | 1101165327 | 131715 | SRX21207459 | SRS18464928 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94274 | 0.83776 | 0.12469 | 0.10926 | 0.71752 | 0.73235 | 0.47225 | 0.46096 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24608 | 24608 | SRR25475204 | SRX21207459 | SRS18464928 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5/10 [PrP BMD5 10 1] | GSM7671230 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5/10 [PrP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5/10 | GSM7671230 | GSM7671230: Zebrafish PrP BMD5/10 [PrP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671230 r1 | GSM7671230 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_10_1_4.fq.gz PrP_BMD5_10_1_3.fq.gz | fastq fastq | 2952201906.0 | 9775503.0 | GSM7671230 r2 | 0:151 1:151 | A:846361785;C:642990303;G:682081110;T:780762283;N:6425 | 151 | 151 | 846361785 | 642990303 | 682081110 | 780762283 | 6425 | SRX21207459 | SRS18464928 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9411 | 0.86904 | 0.12259 | 0.11244 | 0.71392 | 0.72498 | 0.47116 | 0.47213 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24609 | 24609 | SRR25475205 | SRX21207458 | SRS18464927 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 3] | GSM7671229 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671229 | GSM7671229: Zebrafish PrP BMD5 [PrP BMD5 3]; Danio rerio; RNA Seq | GSM7671229 r1 | GSM7671229 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_3_1.fq.gz PrP_BMD5_3_2.fq.gz | fastq fastq | 2629615774.0 | 8707337.0 | GSM7671229 r1 | 0:151 1:151 | A:672958732;C:650029361;G:685902591;T:620641878;N:83212 | 151 | 151 | 672958732 | 650029361 | 685902591 | 620641878 | 83212 | SRX21207458 | SRS18464927 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.96303 | 0.96205 | 0.15116 | 0.14889 | 0.74101 | 0.74548 | 0.57303 | 0.57751 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24610 | 24610 | SRR25475206 | SRX21207458 | SRS18464927 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 3] | GSM7671229 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671229 | GSM7671229: Zebrafish PrP BMD5 [PrP BMD5 3]; Danio rerio; RNA Seq | GSM7671229 r1 | GSM7671229 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_3_3.fq.gz PrP_BMD5_3_4.fq.gz | fastq fastq | 3949175782.0 | 13076741.0 | GSM7671229 r2 | 0:151 1:151 | A:1009211118;C:979393371;G:1019201024;T:941361479;N:8790 | 151 | 151 | 1009211118 | 979393371 | 1019201024 | 941361479 | 8790 | SRX21207458 | SRS18464927 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.96187 | 0.96117 | 0.14636 | 0.14393 | 0.73813 | 0.74357 | 0.55833 | 0.54801 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24611 | 24611 | SRR25475207 | SRX21207457 | SRS18464926 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 2] | GSM7671228 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671228 | GSM7671228: Zebrafish PrP BMD5 [PrP BMD5 2]; Danio rerio; RNA Seq | GSM7671228 r1 | GSM7671228 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_2_1.fq.gz PrP_BMD5_2_3.fq.gz | fastq fastq | 3744054362.0 | 12397531.0 | GSM7671228 r1 | 0:151 1:151 | A:1046548811;C:825316142;G:923103248;T:948967256;N:118905 | 151 | 151 | 1046548811 | 825316142 | 923103248 | 948967256 | 118905 | SRX21207457 | SRS18464926 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9498 | 0.9466 | 0.09201 | 0.09131 | 0.70749 | 0.71506 | 0.44879 | 0.45356 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24612 | 24612 | SRR25475208 | SRX21207457 | SRS18464926 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 2] | GSM7671228 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671228 | GSM7671228: Zebrafish PrP BMD5 [PrP BMD5 2]; Danio rerio; RNA Seq | GSM7671228 r1 | GSM7671228 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_2_4.fq.gz PrP_BMD5_2_2.fq.gz | fastq fastq | 2834446066.0 | 9385583.0 | GSM7671228 r2 | 0:151 1:151 | A:793660024;C:632067365;G:686377801;T:722334752;N:6124 | 151 | 151 | 793660024 | 632067365 | 686377801 | 722334752 | 6124 | SRX21207457 | SRS18464926 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95049 | 0.94632 | 0.09253 | 0.09174 | 0.70818 | 0.71612 | 0.44666 | 0.45596 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24613 | 24613 | SRR25475209 | SRX21207456 | SRS18464925 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 1] | GSM7671227 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671227 | GSM7671227: Zebrafish PrP BMD5 [PrP BMD5 1]; Danio rerio; RNA Seq | GSM7671227 r1 | GSM7671227 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_1_1.fq.gz PrP_BMD5_1_2.fq.gz | fastq fastq | 3340124530.0 | 11060015.0 | GSM7671227 r1 | 0:151 1:151 | A:957829723;C:716152911;G:809681516;T:856354060;N:106320 | 151 | 151 | 957829723 | 716152911 | 809681516 | 856354060 | 106320 | SRX21207456 | SRS18464925 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94378 | 0.93571 | 0.10991 | 0.11032 | 0.71206 | 0.72214 | 0.45578 | 0.44853 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24614 | 24614 | SRR25475210 | SRX21207456 | SRS18464925 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish PrP BMD5 [PrP BMD5 1] | GSM7671227 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5|geo loc name:missing|collection date:missing | Zebrafish PrP BMD5 [PrP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:PrP BMD5 | GSM7671227 | GSM7671227: Zebrafish PrP BMD5 [PrP BMD5 1]; Danio rerio; RNA Seq | GSM7671227 r1 | GSM7671227 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | PrP_BMD5_1_3.fq.gz PrP_BMD5_1_4.fq.gz | fastq fastq | 2589508060.0 | 8574530.0 | GSM7671227 r2 | 0:151 1:151 | A:743364548;C:559167183;G:621696228;T:665273843;N:6258 | 151 | 151 | 743364548 | 559167183 | 621696228 | 665273843 | 6258 | SRX21207456 | SRS18464925 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94424 | 0.93574 | 0.10895 | 0.1074 | 0.70796 | 0.7189 | 0.45538 | 0.45171 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24615 | 24615 | SRR25475211 | SRX21207455 | SRS18464924 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/50 [EtP BMD5 50 3] | GSM7671226 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/50 [EtP BMD5 50 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50 | GSM7671226 | GSM7671226: Zebrafish EtP BMD5/50 [EtP BMD5 50 3]; Danio rerio; RNA Seq | GSM7671226 r1 | GSM7671226 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_50_3_1.fq.gz EtP_BMD5_50_3_2.fq.gz | fastq fastq | 12326499346.0 | 40816223.0 | GSM7671226 r1 | 0:151 1:151 | A:3465072251;C:2766110070;G:2948834852;T:3146092010;N:390163 | 151 | 151 | 3465072251 | 2766110070 | 2948834852 | 3146092010 | 390163 | SRX21207455 | SRS18464924 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95355 | 0.95009 | 0.08714 | 0.08568 | 0.70782 | 0.71589 | 0.45241 | 0.44173 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24616 | 24616 | SRR25475212 | SRX21207454 | SRS18464923 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/50 [EtP BMD5 50 2] | GSM7671225 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/50 [EtP BMD5 50 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50 | GSM7671225 | GSM7671225: Zebrafish EtP BMD5/50 [EtP BMD5 50 2]; Danio rerio; RNA Seq | GSM7671225 r1 | GSM7671225 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_50_2_1.fq.gz EtP_BMD5_50_2_2.fq.gz | fastq fastq | 5873726350.0 | 19449425.0 | GSM7671225 r1 | 0:151 1:151 | A:1639375920;C:1316625633;G:1408239211;T:1509300317;N:185269 | 151 | 151 | 1639375920 | 1316625633 | 1408239211 | 1509300317 | 185269 | SRX21207454 | SRS18464923 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95095 | 0.948 | 0.0908 | 0.09017 | 0.70721 | 0.71224 | 0.45389 | 0.44586 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24617 | 24617 | SRR25475213 | SRX21207454 | SRS18464923 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/50 [EtP BMD5 50 2] | GSM7671225 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/50 [EtP BMD5 50 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50 | GSM7671225 | GSM7671225: Zebrafish EtP BMD5/50 [EtP BMD5 50 2]; Danio rerio; RNA Seq | GSM7671225 r1 | GSM7671225 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_50_2_3.fq.gz EtP_BMD5_50_2_4.fq.gz | fastq fastq | 2920857930.0 | 9671715.0 | GSM7671225 r2 | 0:151 1:151 | A:813299743;C:659443837;G:696023886;T:752084294;N:6170 | 151 | 151 | 813299743 | 659443837 | 696023886 | 752084294 | 6170 | SRX21207454 | SRS18464923 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95323 | 0.94979 | 0.08949 | 0.08869 | 0.70698 | 0.71352 | 0.45222 | 0.45353 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24618 | 24618 | SRR25475214 | SRX21207453 | SRS18464922 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/50 [EtP BMD5 50 1] | GSM7671224 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/50 [EtP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50 | GSM7671224 | GSM7671224: Zebrafish EtP BMD5/50 [EtP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671224 r1 | GSM7671224 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_50_1_1.fq.gz EtP_BMD5_50_1_2.fq.gz | fastq fastq | 3025090814.0 | 10016857.0 | GSM7671224 r1 | 0:151 1:151 | A:843465525;C:670123195;G:725506632;T:785899023;N:96439 | 151 | 151 | 843465525 | 670123195 | 725506632 | 785899023 | 96439 | SRX21207453 | SRS18464922 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.83589 | 0.94217 | 0.09452 | 0.1077 | 0.72299 | 0.71587 | 0.46107 | 0.45633 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24619 | 24619 | SRR25475215 | SRX21207453 | SRS18464922 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/50 [EtP BMD5 50 1] | GSM7671224 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/50 [EtP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/50 | GSM7671224 | GSM7671224: Zebrafish EtP BMD5/50 [EtP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671224 r1 | GSM7671224 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_50_1_3.fq.gz EtP_BMD5_50_1_4.fq.gz | fastq fastq | 2444467124.0 | 8094262.0 | GSM7671224 r2 | 0:151 1:151 | A:679461384;C:546010997;G:581087164;T:637902414;N:5165 | 151 | 151 | 679461384 | 546010997 | 581087164 | 637902414 | 5165 | SRX21207453 | SRS18464922 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.87197 | 0.94213 | 0.1003 | 0.10863 | 0.71616 | 0.71317 | 0.45283 | 0.45457 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24620 | 24620 | SRR25475216 | SRX21207452 | SRS18464921 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/10 [EtP BMD5 10 3] | GSM7671223 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/10 [EtP BMD5 10 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10 | GSM7671223 | GSM7671223: Zebrafish EtP BMD5/10 [EtP BMD5 10 3]; Danio rerio; RNA Seq | GSM7671223 r1 | GSM7671223 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_10_3_1.fq.gz EtP_BMD5_10_3_2.fq.gz | fastq fastq | 9653108974.0 | 31963937.0 | GSM7671223 r1 | 0:151 1:151 | A:2697568973;C:2165083953;G:2288959836;T:2501191246;N:304966 | 151 | 151 | 2697568973 | 2165083953 | 2288959836 | 2501191246 | 304966 | SRX21207452 | SRS18464921 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95172 | 0.95023 | 0.08652 | 0.0862 | 0.70619 | 0.71076 | 0.45447 | 0.45094 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24621 | 24621 | SRR25475217 | SRX21207451 | SRS18464920 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/10 [EtP BMD5 10 2] | GSM7671222 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/10 [EtP BMD5 10 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10 | GSM7671222 | GSM7671222: Zebrafish EtP BMD5/10 [EtP BMD5 10 2]; Danio rerio; RNA Seq | GSM7671222 r1 | GSM7671222 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_10_2_1.fq.gz EtP_BMD5_10_2_3.fq.gz | fastq fastq | 5341647952.0 | 17687576.0 | GSM7671222 r1 | 0:151 1:151 | A:1430194079;C:1246082391;G:1309862164;T:1355339151;N:170167 | 151 | 151 | 1430194079 | 1246082391 | 1309862164 | 1355339151 | 170167 | SRX21207451 | SRS18464920 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95672 | 0.95646 | 0.09343 | 0.09169 | 0.715 | 0.71644 | 0.44995 | 0.46948 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24622 | 24622 | SRR25475218 | SRX21207451 | SRS18464920 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/10 [EtP BMD5 10 2] | GSM7671222 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/10 [EtP BMD5 10 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10 | GSM7671222 | GSM7671222: Zebrafish EtP BMD5/10 [EtP BMD5 10 2]; Danio rerio; RNA Seq | GSM7671222 r1 | GSM7671222 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_10_2_2.fq.gz EtP_BMD5_10_2_4.fq.gz | fastq fastq | 3095850924.0 | 10251162.0 | GSM7671222 r2 | 0:151 1:151 | A:825080641;C:727003748;G:754816513;T:788943347;N:6675 | 151 | 151 | 825080641 | 727003748 | 754816513 | 788943347 | 6675 | SRX21207451 | SRS18464920 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95773 | 0.95746 | 0.09154 | 0.09045 | 0.71145 | 0.71256 | 0.46379 | 0.46536 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24623 | 24623 | SRR25475219 | SRX21207450 | SRS18464919 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/10 [EtP BMD5 10 1] | GSM7671221 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/10 [EtP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10 | GSM7671221 | GSM7671221: Zebrafish EtP BMD5/10 [EtP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671221 r1 | GSM7671221 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_10_1_1.fq.gz EtP_BMD5_10_1_2.fq.gz | fastq fastq | 3224223272.0 | 10676236.0 | GSM7671221 r1 | 0:151 1:151 | A:898136457;C:705998538;G:782593577;T:837393065;N:101635 | 151 | 151 | 898136457 | 705998538 | 782593577 | 837393065 | 101635 | SRX21207450 | SRS18464919 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94431 | 0.94367 | 0.11343 | 0.11295 | 0.71238 | 0.71439 | 0.46018 | 0.45575 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24624 | 24624 | SRR25475220 | SRX21207450 | SRS18464919 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5/10 [EtP BMD5 10 1] | GSM7671221 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5/10 [EtP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5/10 | GSM7671221 | GSM7671221: Zebrafish EtP BMD5/10 [EtP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671221 r1 | GSM7671221 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_10_1_3.fq.gz EtP_BMD5_10_1_4.fq.gz | fastq fastq | 2881317070.0 | 9540785.0 | GSM7671221 r2 | 0:151 1:151 | A:802691268;C:638869913;G:685114354;T:754635149;N:6386 | 151 | 151 | 802691268 | 638869913 | 685114354 | 754635149 | 6386 | SRX21207450 | SRS18464919 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94507 | 0.94452 | 0.11308 | 0.11253 | 0.70694 | 0.71054 | 0.45347 | 0.45385 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24625 | 24625 | SRR25475221 | SRX21207449 | SRS18464918 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5 [EtP BMD5 3] | GSM7671220 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5 [EtP BMD5 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5 | GSM7671220 | GSM7671220: Zebrafish EtP BMD5 [EtP BMD5 3]; Danio rerio; RNA Seq | GSM7671220 r1 | GSM7671220 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_3_1.fq.gz EtP_BMD5_3_2.fq.gz | fastq fastq | 6513209840.0 | 21566920.0 | GSM7671220 r1 | 0:151 1:151 | A:1838683121;C:1445463908;G:1536948771;T:1691910424;N:203616 | 151 | 151 | 1838683121 | 1445463908 | 1536948771 | 1691910424 | 203616 | SRX21207449 | SRS18464918 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94921 | 0.94751 | 0.09226 | 0.09115 | 0.70429 | 0.70907 | 0.45338 | 0.45104 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24626 | 24626 | SRR25475222 | SRX21207448 | SRS18464917 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5 [EtP BMD5 2] | GSM7671219 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5 [EtP BMD5 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5 | GSM7671219 | GSM7671219: Zebrafish EtP BMD5 [EtP BMD5 2]; Danio rerio; RNA Seq | GSM7671219 r1 | GSM7671219 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_2_1.fq.gz EtP_BMD5_2_2.fq.gz | fastq fastq | 4443955368.0 | 14715084.0 | GSM7671219 r1 | 0:151 1:151 | A:1226532150;C:1002488064;G:1058104219;T:1156690900;N:140035 | 151 | 151 | 1226532150 | 1002488064 | 1058104219 | 1156690900 | 140035 | SRX21207448 | SRS18464917 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95173 | 0.95111 | 0.09256 | 0.09128 | 0.70469 | 0.7093 | 0.44316 | 0.44626 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24627 | 24627 | SRR25475223 | SRX21207448 | SRS18464917 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5 [EtP BMD5 2] | GSM7671219 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5 [EtP BMD5 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5 | GSM7671219 | GSM7671219: Zebrafish EtP BMD5 [EtP BMD5 2]; Danio rerio; RNA Seq | GSM7671219 r1 | GSM7671219 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_2_3.fq.gz EtP_BMD5_2_4.fq.gz | fastq fastq | 3368297808.0 | 11153304.0 | GSM7671219 r2 | 0:151 1:151 | A:924217123;C:766145954;G:797666843;T:880260403;N:7485 | 151 | 151 | 924217123 | 766145954 | 797666843 | 880260403 | 7485 | SRX21207448 | SRS18464917 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95185 | 0.95089 | 0.09135 | 0.08974 | 0.70453 | 0.70692 | 0.44872 | 0.45596 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24628 | 24628 | SRR25475224 | SRX21207447 | SRS18464916 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5 [EtP BMD5 1] | GSM7671218 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5 [EtP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5 | GSM7671218 | GSM7671218: Zebrafish EtP BMD5 [EtP BMD5 1]; Danio rerio; RNA Seq | GSM7671218 r1 | GSM7671218 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_1_1.fq.gz EtP_BMD5_1_2.fq.gz | fastq fastq | 2340650396.0 | 7750498.0 | GSM7671218 r1 | 0:151 1:151 | A:667132609;C:510116860;G:548591619;T:614735275;N:74033 | 151 | 151 | 667132609 | 510116860 | 548591619 | 614735275 | 74033 | SRX21207447 | SRS18464916 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94031 | 0.93918 | 0.11457 | 0.11486 | 0.71096 | 0.71482 | 0.46017 | 0.45386 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24629 | 24629 | SRR25475225 | SRX21207447 | SRS18464916 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish EtP BMD5 [EtP BMD5 1] | GSM7671218 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5|geo loc name:missing|collection date:missing | Zebrafish EtP BMD5 [EtP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:EtP BMD5 | GSM7671218 | GSM7671218: Zebrafish EtP BMD5 [EtP BMD5 1]; Danio rerio; RNA Seq | GSM7671218 r1 | GSM7671218 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | EtP_BMD5_1_3.fq.gz EtP_BMD5_1_4.fq.gz | fastq fastq | 3046691364.0 | 10088382.0 | GSM7671218 r2 | 0:151 1:151 | A:865839573;C:668919023;G:709644830;T:802281652;N:6286 | 151 | 151 | 865839573 | 668919023 | 709644830 | 802281652 | 6286 | SRX21207447 | SRS18464916 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9416 | 0.93999 | 0.11428 | 0.11391 | 0.70816 | 0.71376 | 0.45095 | 0.45554 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24630 | 24630 | SRR25475226 | SRX21207446 | SRS18464915 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 3] | GSM7671217 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671217 | GSM7671217: Zebrafish MtP BMD5/50 [MtP BMD5 50 3]; Danio rerio; RNA Seq | GSM7671217 r1 | GSM7671217 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_3_2.fq.gz MtP_BMD5_50_3_1.fq.gz | fastq fastq | 3653327522.0 | 12097111.0 | GSM7671217 r1 | 0:151 1:151 | A:995366744;C:831318635;G:873618716;T:952906846;N:116581 | 151 | 151 | 995366744 | 831318635 | 873618716 | 952906846 | 116581 | SRX21207446 | SRS18464915 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95243 | 0.95252 | 0.09088 | 0.08971 | 0.7167 | 0.71711 | 0.45455 | 0.44644 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24631 | 24631 | SRR25475227 | SRX21207446 | SRS18464915 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 3] | GSM7671217 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671217 | GSM7671217: Zebrafish MtP BMD5/50 [MtP BMD5 50 3]; Danio rerio; RNA Seq | GSM7671217 r1 | GSM7671217 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_3_3.fq.gz MtP_BMD5_50_3_4.fq.gz | fastq fastq | 3423528474.0 | 11336187.0 | GSM7671217 r2 | 0:151 1:151 | A:928366145;C:784910903;G:813824790;T:896419194;N:7442 | 151 | 151 | 928366145 | 784910903 | 813824790 | 896419194 | 7442 | SRX21207446 | SRS18464915 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95366 | 0.9537 | 0.08926 | 0.08783 | 0.71423 | 0.71488 | 0.44252 | 0.44528 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24632 | 24632 | SRR25475228 | SRX21207445 | SRS18464914 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 2] | GSM7671216 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671216 | GSM7671216: Zebrafish MtP BMD5/50 [MtP BMD5 50 2]; Danio rerio; RNA Seq | GSM7671216 r1 | GSM7671216 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_2_1.fq.gz MtP_BMD5_50_2_2.fq.gz | fastq fastq | 4942474922.0 | 16365811.0 | GSM7671216 r1 | 0:151 1:151 | A:1353408937;C:1120658999;G:1177996657;T:1290253217;N:157112 | 151 | 151 | 1353408937 | 1120658999 | 1177996657 | 1290253217 | 157112 | SRX21207445 | SRS18464914 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95342 | 0.9531 | 0.08768 | 0.0872 | 0.71603 | 0.71741 | 0.4477 | 0.45194 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24633 | 24633 | SRR25475229 | SRX21207445 | SRS18464914 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 2] | GSM7671216 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671216 | GSM7671216: Zebrafish MtP BMD5/50 [MtP BMD5 50 2]; Danio rerio; RNA Seq | GSM7671216 r1 | GSM7671216 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_2_4.fq.gz MtP_BMD5_50_2_3.fq.gz | fastq fastq | 3002985622.0 | 9943661.0 | GSM7671216 r2 | 0:151 1:151 | A:819177253;C:685416613;G:712807034;T:785577695;N:7027 | 151 | 151 | 819177253 | 685416613 | 712807034 | 785577695 | 7027 | SRX21207445 | SRS18464914 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95358 | 0.95373 | 0.08626 | 0.08506 | 0.71539 | 0.71737 | 0.44723 | 0.45008 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24634 | 24634 | SRR25475230 | SRX21207444 | SRS18464913 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 1] | GSM7671215 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671215 | GSM7671215: Zebrafish MtP BMD5/50 [MtP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671215 r1 | GSM7671215 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_1_1.fq.gz MtP_BMD5_50_1_2.fq.gz | fastq fastq | 5572679764.0 | 18452582.0 | GSM7671215 r1 | 0:151 1:151 | A:1572978393;C:1231505384;G:1304580144;T:1463439694;N:176149 | 151 | 151 | 1572978393 | 1231505384 | 1304580144 | 1463439694 | 176149 | SRX21207444 | SRS18464913 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94618 | 0.94569 | 0.10995 | 0.10957 | 0.71208 | 0.71577 | 0.44248 | 0.45317 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24635 | 24635 | SRR25475231 | SRX21207444 | SRS18464913 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/50 [MtP BMD5 50 1] | GSM7671215 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/50 [MtP BMD5 50 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/50 | GSM7671215 | GSM7671215: Zebrafish MtP BMD5/50 [MtP BMD5 50 1]; Danio rerio; RNA Seq | GSM7671215 r1 | GSM7671215 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_50_1_3.fq.gz MtP_BMD5_50_1_4.fq.gz | fastq fastq | 3433554572.0 | 11369386.0 | GSM7671215 r2 | 0:151 1:151 | A:966269363;C:763349843;G:801297479;T:902630496;N:7391 | 151 | 151 | 966269363 | 763349843 | 801297479 | 902630496 | 7391 | SRX21207444 | SRS18464913 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94553 | 0.94332 | 0.10986 | 0.10805 | 0.70989 | 0.71388 | 0.45838 | 0.45123 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24636 | 24636 | SRR25475232 | SRX21207443 | SRS18464912 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 3] | GSM7671214 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671214 | GSM7671214: Zebrafish MtP BMD5/10 [MtP BMD5 10 3]; Danio rerio; RNA Seq | GSM7671214 r1 | GSM7671214 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_3_1.fq.gz MtP_BMD5_10_3_2.fq.gz | fastq fastq | 5569270486.0 | 18441293.0 | GSM7671214 r1 | 0:151 1:151 | A:1574836056;C:1234020787;G:1290444481;T:1469794057;N:175105 | 151 | 151 | 1574836056 | 1234020787 | 1290444481 | 1469794057 | 175105 | SRX21207443 | SRS18464912 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95004 | 0.94806 | 0.10109 | 0.10024 | 0.71088 | 0.71415 | 0.45842 | 0.43735 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24637 | 24637 | SRR25475233 | SRX21207443 | SRS18464912 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 3] | GSM7671214 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671214 | GSM7671214: Zebrafish MtP BMD5/10 [MtP BMD5 10 3]; Danio rerio; RNA Seq | GSM7671214 r1 | GSM7671214 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_3_3.fq.gz MtP_BMD5_10_3_4.fq.gz | fastq fastq | 2514406700.0 | 8325850.0 | GSM7671214 r2 | 0:151 1:151 | A:708216865;C:560027758;G:582256307;T:663900270;N:5500 | 151 | 151 | 708216865 | 560027758 | 582256307 | 663900270 | 5500 | SRX21207443 | SRS18464912 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94944 | 0.94814 | 0.10054 | 0.10067 | 0.70751 | 0.71246 | 0.45622 | 0.44451 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24638 | 24638 | SRR25475234 | SRX21207442 | SRS18464911 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 2] | GSM7671213 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671213 | GSM7671213: Zebrafish MtP BMD5/10 [MtP BMD5 10 2]; Danio rerio; RNA Seq | GSM7671213 r1 | GSM7671213 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_2_1.fq.gz MtP_BMD5_10_2_2.fq.gz | fastq fastq | 3506823396.0 | 11611998.0 | GSM7671213 r1 | 0:151 1:151 | A:982455627;C:781917114;G:848218674;T:894124856;N:107125 | 151 | 151 | 982455627 | 781917114 | 848218674 | 894124856 | 107125 | SRX21207442 | SRS18464911 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9504 | 0.94715 | 0.09519 | 0.09469 | 0.71147 | 0.718 | 0.44922 | 0.43458 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24639 | 24639 | SRR25475235 | SRX21207442 | SRS18464911 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 2] | GSM7671213 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671213 | GSM7671213: Zebrafish MtP BMD5/10 [MtP BMD5 10 2]; Danio rerio; RNA Seq | GSM7671213 r1 | GSM7671213 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_2_3.fq.gz MtP_BMD5_10_2_4.fq.gz | fastq fastq | 2523360094.0 | 8355497.0 | GSM7671213 r2 | 0:151 1:151 | A:705451559;C:567104395;G:605344307;T:645454842;N:4991 | 151 | 151 | 705451559 | 567104395 | 605344307 | 645454842 | 4991 | SRX21207442 | SRS18464911 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95062 | 0.94751 | 0.09472 | 0.094 | 0.71005 | 0.71666 | 0.45245 | 0.44889 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24640 | 24640 | SRR25475236 | SRX21207441 | SRS18464910 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 1] | GSM7671212 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671212 | GSM7671212: Zebrafish MtP BMD5/10 [MtP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671212 r1 | GSM7671212 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_1_1.fq.gz MtP_BMD5_10_1_2.fq.gz | fastq fastq | 4528464330.0 | 14994915.0 | GSM7671212 r1 | 0:151 1:151 | A:1261030694;C:1015640347;G:1058184835;T:1193464002;N:144452 | 151 | 151 | 1261030694 | 1015640347 | 1058184835 | 1193464002 | 144452 | SRX21207441 | SRS18464910 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9473 | 0.94598 | 0.11708 | 0.11509 | 0.71364 | 0.71522 | 0.4646 | 0.46444 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24641 | 24641 | SRR25475237 | SRX21207441 | SRS18464910 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5/10 [MtP BMD5 10 1] | GSM7671212 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5/10 [MtP BMD5 10 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5/10 | GSM7671212 | GSM7671212: Zebrafish MtP BMD5/10 [MtP BMD5 10 1]; Danio rerio; RNA Seq | GSM7671212 r1 | GSM7671212 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_10_1_3.fq.gz MtP_BMD5_10_1_4.fq.gz | fastq fastq | 2980367030.0 | 9868765.0 | GSM7671212 r2 | 0:151 1:151 | A:825558450;C:671536928;G:694866440;T:788398550;N:6662 | 151 | 151 | 825558450 | 671536928 | 694866440 | 788398550 | 6662 | SRX21207441 | SRS18464910 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94762 | 0.9469 | 0.11432 | 0.11281 | 0.71001 | 0.71297 | 0.46658 | 0.45541 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24642 | 24642 | SRR25475238 | SRX21207440 | SRS18464909 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5 [MtP BMD5 3] | GSM7671211 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5 [MtP BMD5 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5 | GSM7671211 | GSM7671211: Zebrafish MtP BMD5 [MtP BMD5 3]; Danio rerio; RNA Seq | GSM7671211 r1 | GSM7671211 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_3_1.fq.gz MtP_BMD5_3_2.fq.gz | fastq fastq | 4936487470.0 | 16345985.0 | GSM7671211 r1 | 0:151 1:151 | A:1378752654;C:1113742094;G:1158863879;T:1284972892;N:155951 | 151 | 151 | 1378752654 | 1113742094 | 1158863879 | 1284972892 | 155951 | SRX21207440 | SRS18464909 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95301 | 0.95122 | 0.0955 | 0.0941 | 0.71208 | 0.71648 | 0.44704 | 0.44817 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24643 | 24643 | SRR25475239 | SRX21207440 | SRS18464909 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5 [MtP BMD5 3] | GSM7671211 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5 [MtP BMD5 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5 | GSM7671211 | GSM7671211: Zebrafish MtP BMD5 [MtP BMD5 3]; Danio rerio; RNA Seq | GSM7671211 r1 | GSM7671211 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_3_3.fq.gz MtP_BMD5_3_4.fq.gz | fastq fastq | 3298411686.0 | 10921893.0 | GSM7671211 r2 | 0:151 1:151 | A:917164468;C:748498488;G:774036441;T:858705230;N:7059 | 151 | 151 | 917164468 | 748498488 | 774036441 | 858705230 | 7059 | SRX21207440 | SRS18464909 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95205 | 0.95054 | 0.09425 | 0.09329 | 0.71011 | 0.71455 | 0.44566 | 0.44912 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24644 | 24644 | SRR25475240 | SRX21207439 | SRS18464908 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5 [MtP BMD5 2] | GSM7671210 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5 [MtP BMD5 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5 | GSM7671210 | GSM7671210: Zebrafish MtP BMD5 [MtP BMD5 2]; Danio rerio; RNA Seq | GSM7671210 r1 | GSM7671210 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_2_1.fq.gz MtP_BMD5_2_2.fq.gz | fastq fastq | 6227362008.0 | 20620404.0 | GSM7671210 r1 | 0:151 1:151 | A:1715937364;C:1386359386;G:1515578719;T:1609287962;N:198577 | 151 | 151 | 1715937364 | 1386359386 | 1515578719 | 1609287962 | 198577 | SRX21207439 | SRS18464908 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.9491 | 0.94828 | 0.10169 | 0.10078 | 0.71399 | 0.71605 | 0.45429 | 0.454 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24645 | 24645 | SRR25475241 | SRX21207438 | SRS18464907 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5 [MtP BMD5 1] | GSM7671209 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5 [MtP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5 | GSM7671209 | GSM7671209: Zebrafish MtP BMD5 [MtP BMD5 1]; Danio rerio; RNA Seq | GSM7671209 r1 | GSM7671209 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_1_1.fq.gz MtP_BMD5_1_4.fq.gz | fastq fastq | 4052874428.0 | 13420114.0 | GSM7671209 r1 | 0:151 1:151 | A:1131227099;C:867529007;G:1014888508;T:1039101737;N:128077 | 151 | 151 | 1131227099 | 867529007 | 1014888508 | 1039101737 | 128077 | SRX21207438 | SRS18464907 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94427 | 0.94289 | 0.11676 | 0.11646 | 0.71587 | 0.72013 | 0.4544 | 0.45822 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24646 | 24646 | SRR25475242 | SRX21207438 | SRS18464907 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish MtP BMD5 [MtP BMD5 1] | GSM7671209 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5|geo loc name:missing|collection date:missing | Zebrafish MtP BMD5 [MtP BMD5 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:MtP BMD5 | GSM7671209 | GSM7671209: Zebrafish MtP BMD5 [MtP BMD5 1]; Danio rerio; RNA Seq | GSM7671209 r1 | GSM7671209 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | MtP_BMD5_1_2.fq.gz MtP_BMD5_1_3.fq.gz | fastq fastq | 3419102060.0 | 11321530.0 | GSM7671209 r2 | 0:151 1:151 | A:962312797;C:746662074;G:817866377;T:892253758;N:7054 | 151 | 151 | 962312797 | 746662074 | 817866377 | 892253758 | 7054 | SRX21207438 | SRS18464907 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94437 | 0.94159 | 0.11604 | 0.11533 | 0.7122 | 0.71697 | 0.45308 | 0.45718 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24647 | 24647 | SRR25475243 | SRX21207437 | SRS18464906 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish Control [C 3] | GSM7671208 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control|geo loc name:missing|collection date:missing | Zebrafish Control [C 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control | GSM7671208 | GSM7671208: Zebrafish Control [C 3]; Danio rerio; RNA Seq | GSM7671208 r1 | GSM7671208 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | C_3_1.fq.gz C_3_2.fq.gz | fastq fastq | 5057829560.0 | 16747780.0 | GSM7671208 r1 | 0:151 1:151 | A:1402165693;C:1118939077;G:1238989668;T:1297578003;N:157119 | 151 | 151 | 1402165693 | 1118939077 | 1238989668 | 1297578003 | 157119 | SRX21207437 | SRS18464906 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95294 | 0.95134 | 0.09354 | 0.09252 | 0.71758 | 0.72255 | 0.44734 | 0.44399 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24648 | 24648 | SRR25475244 | SRX21207437 | SRS18464906 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish Control [C 3] | GSM7671208 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control|geo loc name:missing|collection date:missing | Zebrafish Control [C 3] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control | GSM7671208 | GSM7671208: Zebrafish Control [C 3]; Danio rerio; RNA Seq | GSM7671208 r1 | GSM7671208 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | C_3_3.fq.gz C_3_4.fq.gz | fastq fastq | 2444105026.0 | 8093063.0 | GSM7671208 r2 | 0:151 1:151 | A:677519922;C:547933936;G:588011673;T:630634167;N:5328 | 151 | 151 | 677519922 | 547933936 | 588011673 | 630634167 | 5328 | SRX21207437 | SRS18464906 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95279 | 0.95095 | 0.09225 | 0.09186 | 0.71532 | 0.72021 | 0.44267 | 0.42467 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24649 | 24649 | SRR25475245 | SRX21207436 | SRS18464905 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish Control [C 2] | GSM7671207 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control|geo loc name:missing|collection date:missing | Zebrafish Control [C 2] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control | GSM7671207 | GSM7671207: Zebrafish Control [C 2]; Danio rerio; RNA Seq | GSM7671207 r1 | GSM7671207 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | C_2_1.fq.gz C_2_2.fq.gz | fastq fastq | 6798305692.0 | 22510946.0 | GSM7671207 r1 | 0:151 1:151 | A:1815427330;C:1575068301;G:1689634001;T:1717960363;N:215697 | 151 | 151 | 1815427330 | 1575068301 | 1689634001 | 1717960363 | 215697 | SRX21207436 | SRS18464905 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.95273 | 0.95222 | 0.10352 | 0.10219 | 0.71806 | 0.71952 | 0.468 | 0.47405 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24650 | 24650 | SRR25475246 | SRX21207435 | SRS18464904 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish Control [C 1] | GSM7671206 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control|geo loc name:missing|collection date:missing | Zebrafish Control [C 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control | GSM7671206 | GSM7671206: Zebrafish Control [C 1]; Danio rerio; RNA Seq | GSM7671206 r1 | GSM7671206 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | C_1_1.fq.gz C_1_2.fq.gz | fastq fastq | 4775780888.0 | 15813844.0 | GSM7671206 r1 | 0:151 1:151 | A:1349640328;C:1033890598;G:1150153417;T:1241944276;N:152269 | 151 | 151 | 1349640328 | 1033890598 | 1150153417 | 1241944276 | 152269 | SRX21207435 | SRS18464904 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.93975 | 0.93846 | 0.11061 | 0.11057 | 0.70796 | 0.7122 | 0.45018 | 0.4485 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24651 | 24651 | SRR25475247 | SRX21207435 | SRS18464904 | SRP452529 | PRJNA1000943 | Transcriptome analysis reveals differences in developmental neurotoxicity mechanism of methyl ethyl and propyl parabens in zebrafish embryos | GSE239773 | Transcriptome Analysis | Limited studies on comparison of developmental neurotoxicity of parabens have been conducted and unharmonized concentrations between phenotypic observations and transcriptomic analysis hamper understanding of their differential molecular mechanism. Developmental toxicity testing was conducted with commonly used methyl MtP ethyl EtP and propyl paraben PrP in zebrafish embryos. Based on benchmark dose 5% BMD5 embryonic mortality based point of departure M PoD values of three parabens were determined and changes in locomotor behavior were evaluated at concentrations of 0 M PoD/50 M PoD/10 and M PoD in which transcriptomic analysis was conducted to explore the underlying neurotoxicity mechanism. Higher long chained parabens were more toxic than short chained parabens as determined by M PoD values of 154.1 72.6 and 24.2 µM for MtP EtP and PrP respectively. While exposure to EtP resulted in hyperactivity no behavior effect was observed by MtP and PrP. Transcriptomics analysis revealed that abnormal behaviors in EtP exposed group are associated with the distinctly enriched pathways in signal transport calcium ion binding and metal binding. In contrast exposure to MtP and PrP mainly disrupted the membrane and transmembrane which are closely linked to abnormal embryonic development rather than neurobehavior changes. According to the changes in expression of signature mRNAs tentative transcriptomic based PoD T PoD values for each paraben were determined as MtP 2.68 µM EtP 3.85 µM and PrP 1.4 µM. Overall design: Comparative gene expression profiling analysis of RNA seq data for zebrafish Danio rerio. This study was supported by Korea Environment Industry & Technology Institute KEITI through "the Technology Development Project for Safety Management of Household Chemical Products" funded by Korea Ministry of Environment MOE grant number 2020002960006. | Zebrafish Control [C 1] | GSM7671206 | source name:Whole body|strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control|geo loc name:missing|collection date:missing | Zebrafish Control [C 1] | Filtered reads quality >20 and length >50 were aligned to the Ensembl reference genome on Danio rerio GCA 000002035.4. Assembly: GCA 000002035.4 Supplementary files format and content: RPKM TPM values | Whole body | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | strain:AB wild type|tissue:Whole body|developmental stage:120 hpf|treatment:Control | GSM7671206 | GSM7671206: Zebrafish Control [C 1]; Danio rerio; RNA Seq | GSM7671206 r1 | GSM7671206 | 1 | The RNA extraction was conducted with RNAzol® reagent Molecular Research Center Inc. Cincinnati OH USA and appropriate amounts >200 ng of RNA were obtained. A KAPA Library Quantification Kit was used to quantify the sequencing library | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP452529 | loader:fastq load.py | C_1_3.fq.gz C_1_4.fq.gz | fastq fastq | 2235109248.0 | 7401024.0 | GSM7671206 r2 | 0:151 1:151 | A:630617292;C:490828084;G:527489424;T:586169387;N:5061 | 151 | 151 | 630617292 | 490828084 | 527489424 | 586169387 | 5061 | SRX21207435 | SRS18464904 | SRA1684601 | Seoul National University of Science and Technology | Seoul National University of Science and Technology | 2 | 0.94126 | 0.94112 | 0.10981 | 0.11011 | 0.70485 | 0.70995 | 0.44139 | 0.45284 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | South Korea | 2023-08-01 | Larval | Larval | Trunk | Surface Structure | ||||||||||||
| 24906 | 24906 | SRR25532497 | SRX21261798 | SRS18515093 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | control1 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.42 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S10 | S10 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | CK1_1.fq.gz CK1_2.fq.gz | fastq fastq | 6650697900.0 | 22168993.0 | CK1 1.fq.gz | 0:150 1:150 | A:1918460669;C:1420936092;G:1412569553;T:1898656995;N:74591 | 150 | 150 | 1918460669 | 1420936092 | 1412569553 | 1898656995 | 74591 | SRX21261798 | SRS18515093 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.91765 | 0.91694 | 0.15569 | 0.15461 | 0.70185 | 0.7027 | 0.47761 | 0.47369 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24907 | 24907 | SRR25532498 | SRX21261797 | SRS18515092 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTH3 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.41 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S9 | S9 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTH3_2.fq.gz MBTH3_1.fq.gz | fastq fastq | 6333332100.0 | 21111107.0 | MBTH3 1.fq.gz | 0:150 1:150 | A:1755718187;C:1429192980;G:1420776066;T:1727550080;N:94787 | 150 | 150 | 1755718187 | 1429192980 | 1420776066 | 1727550080 | 94787 | SRX21261797 | SRS18515092 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.93518 | 0.93355 | 0.11668 | 0.11602 | 0.67799 | 0.67817 | 0.47705 | 0.47875 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24908 | 24908 | SRR25532499 | SRX21261796 | SRS18515091 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTH2 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.40 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S8 | S8 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTH2_1.fq.gz MBTH2_2.fq.gz | fastq fastq | 6373733400.0 | 21245778.0 | MBTH2 1.fq.gz | 0:150 1:150 | A:1775132718;C:1430955007;G:1424605018;T:1742942742;N:97915 | 150 | 150 | 1775132718 | 1430955007 | 1424605018 | 1742942742 | 97915 | SRX21261796 | SRS18515091 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.93081 | 0.93016 | 0.12061 | 0.11947 | 0.68215 | 0.68172 | 0.47956 | 0.48186 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24909 | 24909 | SRR25532500 | SRX21261795 | SRS18515090 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTH1 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.39 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S7 | S7 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTH1_1.fq.gz MBTH1_2.fq.gz | fastq fastq | 6224052600.0 | 20746842.0 | MBTH1 1.fq.gz | 0:150 1:150 | A:1753175301;C:1379045823;G:1371537072;T:1720226102;N:68302 | 150 | 150 | 1753175301 | 1379045823 | 1371537072 | 1720226102 | 68302 | SRX21261795 | SRS18515090 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.9276 | 0.92379 | 0.13642 | 0.13482 | 0.68416 | 0.68479 | 0.47638 | 0.47581 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24910 | 24910 | SRR25532501 | SRX21261794 | SRS18515089 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTM3 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.38 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S6 | S6 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTM3_2.fq.gz MBTM3_1.fq.gz | fastq fastq | 6885667800.0 | 22952226.0 | MBTM3 1.fq.gz | 0:150 1:150 | A:1936367424;C:1526831248;G:1520656271;T:1901736749;N:76108 | 150 | 150 | 1936367424 | 1526831248 | 1520656271 | 1901736749 | 76108 | SRX21261794 | SRS18515089 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.92736 | 0.92516 | 0.12801 | 0.12693 | 0.68982 | 0.69063 | 0.47163 | 0.4612 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24911 | 24911 | SRR25532502 | SRX21261793 | SRS18515088 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTM2 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.37 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S5 | S5 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTM2_1.fq.gz MBTM2_2.fq.gz | fastq fastq | 6529427400.0 | 21764758.0 | MBTM2 1.fq.gz | 0:150 1:150 | A:1808908277;C:1472638598;G:1467975655;T:1779801002;N:103868 | 150 | 150 | 1808908277 | 1472638598 | 1467975655 | 1779801002 | 103868 | SRX21261793 | SRS18515088 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.9296 | 0.93217 | 0.11772 | 0.11735 | 0.68262 | 0.68331 | 0.4724 | 0.4721 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24912 | 24912 | SRR25532503 | SRX21261792 | SRS18515087 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTM1 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.36 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S4 | S4 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTM1_2.fq.gz MBTM1_1.fq.gz | fastq fastq | 6733924800.0 | 22446416.0 | MBTM1 1.fq.gz | 0:150 1:150 | A:1847490053;C:1535661831;G:1528806965;T:1821868439;N:97512 | 150 | 150 | 1847490053 | 1535661831 | 1528806965 | 1821868439 | 97512 | SRX21261792 | SRS18515087 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.93177 | 0.93448 | 0.11165 | 0.11192 | 0.67722 | 0.67823 | 0.47325 | 0.46912 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24913 | 24913 | SRR25532504 | SRX21261791 | SRS18515086 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTL3 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.35 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S3 | S3 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTL3_1.fq.gz MBTL3_2.fq.gz | fastq fastq | 9066238500.0 | 30220795.0 | MBTL3 1.fq.gz | 0:150 1:150 | A:2629692873;C:1932648084;G:1927694770;T:2576111685;N:91088 | 150 | 150 | 2629692873 | 1932648084 | 1927694770 | 2576111685 | 91088 | SRX21261791 | SRS18515086 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.93079 | 0.91809 | 0.1476 | 0.14446 | 0.69201 | 0.69258 | 0.47663 | 0.47687 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24914 | 24914 | SRR25532505 | SRX21261790 | SRS18515085 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | control3 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.44 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S12 | S12 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | CK3_1.fq.gz CK3_2.fq.gz | fastq fastq | 6596041200.0 | 21986804.0 | CK3 1.fq.gz | 0:150 1:150 | A:1886076947;C:1431757712;G:1423068767;T:1855067482;N:70292 | 150 | 150 | 1886076947 | 1431757712 | 1423068767 | 1855067482 | 70292 | SRX21261790 | SRS18515085 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.92168 | 0.92147 | 0.14797 | 0.14768 | 0.68962 | 0.68935 | 0.47874 | 0.48307 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24915 | 24915 | SRR25532506 | SRX21261789 | SRS18515084 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | control2 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.43 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S11 | S11 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | CK2_1.fq.gz CK2_2.fq.gz | fastq fastq | 6749651400.0 | 22498838.0 | CK2 1.fq.gz | 0:150 1:150 | A:1934306700;C:1451979582;G:1445551014;T:1917740723;N:73381 | 150 | 150 | 1934306700 | 1451979582 | 1445551014 | 1917740723 | 73381 | SRX21261789 | SRS18515084 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.92261 | 0.92062 | 0.15096 | 0.14969 | 0.69783 | 0.69702 | 0.48303 | 0.49016 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24916 | 24916 | SRR25532507 | SRX21261788 | SRS18515083 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTL2 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.34 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S2 | S2 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTL2_1.fq.gz MBTL2_2.fq.gz | fastq fastq | 6868354800.0 | 22894516.0 | MBTL2 1.fq.gz | 0:150 1:150 | A:1956017484;C:1493585329;G:1486220640;T:1932456728;N:74619 | 150 | 150 | 1956017484 | 1493585329 | 1486220640 | 1932456728 | 74619 | SRX21261788 | SRS18515083 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.92126 | 0.91908 | 0.14701 | 0.14525 | 0.69394 | 0.69363 | 0.47281 | 0.47636 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 24917 | 24917 | SRR25532508 | SRX21261787 | SRS18515082 | SRP453533 | PRJNA1002570 | MBT induced effects in zebrafish eyes | PRJNA1002570 | Other | We intended to screen the key events in zebrafish larvae post MBT exposure. | MBTL1 | strain:not collected|isolate:not collected|breed:not collected|cultivar:not collected|ecotype:not collected|age:not collected|dev stage:not collected|collection date:2022 11|geo loc name:China: Beijing|sex:not applicable|tissue:whole body|lat lon:39.9 N 116.33 E|sample type:whole organism|BioSampleModel:Model organism or animal | RNAseq of fish | S1 | S1 | normal RNAseq of fish | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP453533 | MBTL1_1.fq.gz MBTL1_2.fq.gz | fastq fastq | 6305127900.0 | 21017093.0 | MBTL1 1.fq.gz | 0:150 1:150 | A:1797030982;C:1364002775;G:1357954929;T:1786051425;N:87789 | 150 | 150 | 1797030982 | 1364002775 | 1357954929 | 1786051425 | 87789 | SRX21261787 | SRS18515082 | SRA1687160 | Chinese Academy of Sciences|RESEARCH CENTER FOR ECO-ENVIRONMENTAL SCIENCES | Chinese Academy of Sciences | 2 | 0.92195 | 0.92138 | 0.14404 | 0.1433 | 0.69656 | 0.69623 | 0.47185 | 0.46936 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2023-08-05 | Undetermined | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 25329 | 25329 | SRR25868071 | SRX21589492 | SRS18767065 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibCGFP4 | GSM7749557 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | sibCGFP4 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP | GSM7749557 | GSM7749557: sibCGFP4; Danio rerio; RNA Seq | GSM7749557 r1 | GSM7749557 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibCGFP4_S46_L002_R1_001.fastq.gz WA-3548-sibCGFP4_S46_L002_R2_001.fastq.gz | fastq fastq | 11996252984.0 | 39722692.0 | GSM7749557 r1 | 0:151 1:151 | A:3208564840;C:2791941387;G:2921724669;T:3073456372;N:565716 | 151 | 151 | 3208564840 | 2791941387 | 2921724669 | 3073456372 | 565716 | SRX21589492 | SRS18767065 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96224 | 0.96334 | 0.07442 | 0.07372 | 0.70595 | 0.70688 | 0.47053 | 0.46853 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25330 | 25330 | SRR25868072 | SRX21589491 | SRS18767064 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibCGFP3 | GSM7749556 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | sibCGFP3 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP | GSM7749556 | GSM7749556: sibCGFP3; Danio rerio; RNA Seq | GSM7749556 r1 | GSM7749556 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibCGFP3_S45_L002_R1_001.fastq.gz WA-3548-sibCGFP3_S45_L002_R2_001.fastq.gz | fastq fastq | 10113421300.0 | 33488150.0 | GSM7749556 r1 | 0:151 1:151 | A:2677217319;C:2366433560;G:2481164832;T:2588131881;N:473708 | 151 | 151 | 2677217319 | 2366433560 | 2481164832 | 2588131881 | 473708 | SRX21589491 | SRS18767064 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96295 | 0.96335 | 0.07275 | 0.07118 | 0.70654 | 0.7092 | 0.45672 | 0.44027 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25331 | 25331 | SRR25868073 | SRX21589490 | SRS18767063 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibCGFP2 | GSM7749555 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | sibCGFP2 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP | GSM7749555 | GSM7749555: sibCGFP2; Danio rerio; RNA Seq | GSM7749555 r1 | GSM7749555 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibCGFP2_S44_L002_R1_001.fastq.gz WA-3548-sibCGFP2_S44_L002_R2_001.fastq.gz | fastq fastq | 10142198578.0 | 33583439.0 | GSM7749555 r1 | 0:151 1:151 | A:2687719512;C:2375571494;G:2493046337;T:2585391111;N:470124 | 151 | 151 | 2687719512 | 2375571494 | 2493046337 | 2585391111 | 470124 | SRX21589490 | SRS18767063 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96241 | 0.96294 | 0.07398 | 0.07262 | 0.70524 | 0.70589 | 0.45777 | 0.46014 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25332 | 25332 | SRR25868074 | SRX21589489 | SRS18767062 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibCGFP1 | GSM7749554 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | sibCGFP1 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ ;Tg503unc:fhl2b T2A EGFP | GSM7749554 | GSM7749554: sibCGFP1; Danio rerio; RNA Seq | GSM7749554 r1 | GSM7749554 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibCGFP1_S43_L002_R1_001.fastq.gz WA-3548-sibCGFP1_S43_L002_R2_001.fastq.gz | fastq fastq | 10994030650.0 | 36404075.0 | GSM7749554 r1 | 0:151 1:151 | A:2911908895;C:2573164804;G:2700790583;T:2807654156;N:512212 | 151 | 151 | 2911908895 | 2573164804 | 2700790583 | 2807654156 | 512212 | SRX21589489 | SRS18767062 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96119 | 0.96215 | 0.07361 | 0.07253 | 0.70632 | 0.7069 | 0.45503 | 0.45981 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25333 | 25333 | SRR25868075 | SRX21589488 | SRS18767059 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibC4 | GSM7749553 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ |geo loc name:missing|collection date:missing | sibC4 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ | GSM7749553 | GSM7749553: sibC4; Danio rerio; RNA Seq | GSM7749553 r1 | GSM7749553 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibC4_S42_L002_R1_001.fastq.gz WA-3548-sibC4_S42_L002_R2_001.fastq.gz | fastq fastq | 11107320816.0 | 36779208.0 | GSM7749553 r1 | 0:151 1:151 | A:2945889871;C:2588267204;G:2719520712;T:2853118433;N:524596 | 151 | 151 | 2945889871 | 2588267204 | 2719520712 | 2853118433 | 524596 | SRX21589488 | SRS18767059 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96098 | 0.96213 | 0.07535 | 0.07463 | 0.70623 | 0.70749 | 0.42034 | 0.43255 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25334 | 25334 | SRR25868076 | SRX21589487 | SRS18767060 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibC3 | GSM7749552 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ |geo loc name:missing|collection date:missing | sibC3 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ | GSM7749552 | GSM7749552: sibC3; Danio rerio; RNA Seq | GSM7749552 r1 | GSM7749552 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibC3_S41_L002_R1_001.fastq.gz WA-3548-sibC3_S41_L002_R2_001.fastq.gz | fastq fastq | 12566811014.0 | 41611957.0 | GSM7749552 r1 | 0:151 1:151 | A:3330340903;C:2960050871;G:3087690864;T:3188143295;N:585081 | 151 | 151 | 3330340903 | 2960050871 | 3087690864 | 3188143295 | 585081 | SRX21589487 | SRS18767060 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.9619 | 0.96201 | 0.08592 | 0.08414 | 0.69581 | 0.69637 | 0.47091 | 0.47561 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25335 | 25335 | SRR25868077 | SRX21589486 | SRS18767057 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibC2 | GSM7749551 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ |geo loc name:missing|collection date:missing | sibC2 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ | GSM7749551 | GSM7749551: sibC2; Danio rerio; RNA Seq | GSM7749551 r1 | GSM7749551 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibC2_S40_L002_R1_001.fastq.gz WA-3548-sibC2_S40_L002_R2_001.fastq.gz | fastq fastq | 9464242402.0 | 31338551.0 | GSM7749551 r1 | 0:151 1:151 | A:2497543137;C:2235078067;G:2319534414;T:2411649747;N:437037 | 151 | 151 | 2497543137 | 2235078067 | 2319534414 | 2411649747 | 437037 | SRX21589486 | SRS18767057 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96464 | 0.965 | 0.06696 | 0.06563 | 0.7138 | 0.71512 | 0.46359 | 0.46601 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25336 | 25336 | SRR25868078 | SRX21589485 | SRS18767061 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | sibC1 | GSM7749550 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ |geo loc name:missing|collection date:missing | sibC1 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd+/ | GSM7749550 | GSM7749550: sibC1; Danio rerio; RNA Seq | GSM7749550 r1 | GSM7749550 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-sibC1_S39_L002_R1_001.fastq.gz WA-3548-sibC1_S39_L002_R2_001.fastq.gz | fastq fastq | 11153872908.0 | 36933354.0 | GSM7749550 r1 | 0:151 1:151 | A:2966120106;C:2600333644;G:2710289968;T:2876608337;N:520853 | 151 | 151 | 2966120106 | 2600333644 | 2710289968 | 2876608337 | 520853 | SRX21589485 | SRS18767061 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96189 | 0.96306 | 0.07632 | 0.07512 | 0.70749 | 0.70818 | 0.46784 | 0.4683 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25337 | 25337 | SRR25868079 | SRX21589484 | SRS18767058 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmdGFP4 | GSM7749549 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | dmdGFP4 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP | GSM7749549 | GSM7749549: dmdGFP4; Danio rerio; RNA Seq | GSM7749549 r1 | GSM7749549 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmdGFP4_S54_L002_R1_001.fastq.gz WA-3548-dmdGFP4_S54_L002_R2_001.fastq.gz | fastq fastq | 6593937762.0 | 21834231.0 | GSM7749549 r1 | 0:151 1:151 | A:1745786828;C:1531704556;G:1637507801;T:1678632967;N:305610 | 151 | 151 | 1745786828 | 1531704556 | 1637507801 | 1678632967 | 305610 | SRX21589484 | SRS18767058 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.9626 | 0.96282 | 0.08653 | 0.08533 | 0.70433 | 0.70636 | 0.47707 | 0.46994 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25338 | 25338 | SRR25868080 | SRX21589483 | SRS18767056 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmdGFP3 | GSM7749548 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | dmdGFP3 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP | GSM7749548 | GSM7749548: dmdGFP3; Danio rerio; RNA Seq | GSM7749548 r1 | GSM7749548 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmdGFP3_S53_L002_R1_001.fastq.gz WA-3548-dmdGFP3_S53_L002_R2_001.fastq.gz | fastq fastq | 9250573476.0 | 30631038.0 | GSM7749548 r1 | 0:151 1:151 | A:2485551140;C:2135752367;G:2259698711;T:2369143289;N:427969 | 151 | 151 | 2485551140 | 2135752367 | 2259698711 | 2369143289 | 427969 | SRX21589483 | SRS18767056 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96118 | 0.96196 | 0.0946 | 0.09271 | 0.69702 | 0.69834 | 0.47168 | 0.47515 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25339 | 25339 | SRR25868081 | SRX21589482 | SRS18767055 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmdGFP2 | GSM7749547 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | dmdGFP2 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP | GSM7749547 | GSM7749547: dmdGFP2; Danio rerio; RNA Seq | GSM7749547 r1 | GSM7749547 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmdGFP2_S52_L002_R1_001.fastq.gz WA-3548-dmdGFP2_S52_L002_R2_001.fastq.gz | fastq fastq | 8584886654.0 | 28426777.0 | GSM7749547 r1 | 0:151 1:151 | A:2310205296;C:1982936514;G:2071907465;T:2219441471;N:395908 | 151 | 151 | 2310205296 | 1982936514 | 2071907465 | 2219441471 | 395908 | SRX21589482 | SRS18767055 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.9586 | 0.95966 | 0.09636 | 0.09473 | 0.69881 | 0.6997 | 0.47446 | 0.47409 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25340 | 25340 | SRR25868082 | SRX21589481 | SRS18767052 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmdGFP1 | GSM7749546 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP|geo loc name:missing|collection date:missing | dmdGFP1 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / ;Tg503unc:fhl2b T2A EGFP | GSM7749546 | GSM7749546: dmdGFP1; Danio rerio; RNA Seq | GSM7749546 r1 | GSM7749546 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmdGFP1_S51_L002_R1_001.fastq.gz WA-3548-dmdGFP1_S51_L002_R2_001.fastq.gz | fastq fastq | 7573189674.0 | 25076787.0 | GSM7749546 r1 | 0:151 1:151 | A:2025587174;C:1735604560;G:1848622101;T:1963022142;N:353697 | 151 | 151 | 2025587174 | 1735604560 | 1848622101 | 1963022142 | 353697 | SRX21589481 | SRS18767052 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.95942 | 0.96073 | 0.08752 | 0.08624 | 0.69863 | 0.69822 | 0.4733 | 0.47454 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25341 | 25341 | SRR25868083 | SRX21589480 | SRS18767054 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmd4 | GSM7749545 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / |geo loc name:missing|collection date:missing | dmd4 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / | GSM7749545 | GSM7749545: dmd4; Danio rerio; RNA Seq | GSM7749545 r1 | GSM7749545 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmd4_S50_L002_R1_001.fastq.gz WA-3548-dmd4_S50_L002_R2_001.fastq.gz | fastq fastq | 9121652998.0 | 30204149.0 | GSM7749545 r1 | 0:151 1:151 | A:2438907102;C:2114952319;G:2225797925;T:2341561511;N:434141 | 151 | 151 | 2438907102 | 2114952319 | 2225797925 | 2341561511 | 434141 | SRX21589480 | SRS18767054 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.961 | 0.96258 | 0.08366 | 0.08276 | 0.69787 | 0.69856 | 0.47181 | 0.46112 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25342 | 25342 | SRR25868084 | SRX21589479 | SRS18767053 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmd3 | GSM7749544 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / |geo loc name:missing|collection date:missing | dmd3 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / | GSM7749544 | GSM7749544: dmd3; Danio rerio; RNA Seq | GSM7749544 r1 | GSM7749544 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmd3_S49_L002_R1_001.fastq.gz WA-3548-dmd3_S49_L002_R2_001.fastq.gz | fastq fastq | 7896671538.0 | 26147919.0 | GSM7749544 r1 | 0:151 1:151 | A:2104101125;C:1828908837;G:1933039401;T:2030257090;N:365085 | 151 | 151 | 2104101125 | 1828908837 | 1933039401 | 2030257090 | 365085 | SRX21589479 | SRS18767053 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96014 | 0.96084 | 0.08575 | 0.08475 | 0.70082 | 0.70108 | 0.47254 | 0.47153 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25343 | 25343 | SRR25868085 | SRX21589478 | SRS18767051 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmd2 | GSM7749543 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / |geo loc name:missing|collection date:missing | dmd2 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / | GSM7749543 | GSM7749543: dmd2; Danio rerio; RNA Seq | GSM7749543 r1 | GSM7749543 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmd2_S48_L002_R1_001.fastq.gz WA-3548-dmd2_S48_L002_R2_001.fastq.gz | fastq fastq | 9484006792.0 | 31403996.0 | GSM7749543 r1 | 0:151 1:151 | A:2518758838;C:2211640185;G:2303907076;T:2449259369;N:441324 | 151 | 151 | 2518758838 | 2211640185 | 2303907076 | 2449259369 | 441324 | SRX21589478 | SRS18767051 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96047 | 0.96128 | 0.09081 | 0.09031 | 0.69603 | 0.69605 | 0.46706 | 0.47077 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25344 | 25344 | SRR25868086 | SRX21589477 | SRS18767050 | SRP457981 | PRJNA1011838 | fhl2b expression ameliorates muscular dystrophy [5dpf trunk] | GSE242135 | Transcriptome Analysis | In muscle dystrophies muscle fibers loose integrity and die leading to significant suffering and a shorter life. Strikingly the extraocular muscles EOMs controlling eye movements are spared and function well despite the disease progression. Although EOMs have been shown to have important differences compared to body musculature the mechanisms underlying this inherent resistance to muscle dystrophies remain largely unknown. Here we demonstrate important differences in gene expression as a response to muscle dystrophies between the EOMs and trunk muscle in zebrafish via transcriptomic profiling. We show that the LIM protein Fhl2 is upregulated in response to knockout of desmin plectin and obscurin intermediate filament proteins causing different muscle dystrophies and contributes to disease protection of the EOMs. Moreover we show that ectopic expression of fhl2b can partially rescue the muscle phenotype in the zebrafish Duchenne muscular dystrophy model sapje significantly improving their survival rate. Therefore fhl2 is a protective agent and a candidate target gene for therapy of muscle dystrophies. Overall design: To examine the effect of fhl2b overexpression in muscle in the background of the dmd/sapje mutant line at 5 dpf | parent bioproject:PRJNA1011837 | pubmed:38431640 | dmd1 | GSM7749542 | source name:5 dpf trunk|tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / |geo loc name:missing|collection date:missing | dmd1 | Sequence reads were mapped to GRCz11 using STAR options: outSAMtype BAM SortedByCoordinate seedSearchStartLmax 12 outFilterScoreMinOverLread 0.3 alignSJoverhangMin 15 outFilterMismatchNmax 33 outFilterMatchNminOverLread 0 outFilterType BySJout outSAMunmapped Within outSAMattributes NH HI AS NM MD outSAMstrandField intronMotif quantMode GeneCounts Read count extraction and normalization were performed using R package DeSEQ2 Assembly: GRCz11 Supplementary files format and content: tab delimited text files include raw counts | 5 dpf trunk | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | WT AB zebrafish used originated from the same line utilized when generating the desma / ;desmb / double mutant. Zebrafish were maintained by standard procedures on a 10/14h dark/light cycle at 28°C | tissue:5 dpf trunk|cell line:dmd: t222a|cell type:zebrafish trunk|genotype:dmd / | GSM7749542 | GSM7749542: dmd1; Danio rerio; RNA Seq | GSM7749542 r1 | GSM7749542 | 1 | Muscle tissue was dissected from freshly sacrificed zebrafish and dissected in RNA later solution from Sigma and stored at 80C. All collected samples were then treated with TRIZOL according to the manufactors description. 400ng total RNA was used for library construction. Illumina TruSeq Stranded mRNA poly A selection | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457981 | loader:fastq load.py | WA-3548-dmd1_S47_L002_R1_001.fastq.gz WA-3548-dmd1_S47_L002_R2_001.fastq.gz | fastq fastq | 8411057568.0 | 27851184.0 | GSM7749542 r1 | 0:151 1:151 | A:2239146475;C:1963458820;G:2046268505;T:2161796444;N:387324 | 151 | 151 | 2239146475 | 1963458820 | 2046268505 | 2161796444 | 387324 | SRX21589477 | SRS18767050 | SRA1703879 | Umeå Univeristy | Umeå Univeristy | 2 | 0.96292 | 0.96424 | 0.07952 | 0.07845 | 0.70473 | 0.70467 | 0.47569 | 0.47555 | 151 | 151 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | poly_a | trueseq | bulk | bulk | bulk | Sweden | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||
| 25369 | 25369 | SRR25869114 | SRX21590526 | SRS18768099 | SRP457982 | PRJNA1011844 | Comparison of zebrafish toxicity among different developmental windows of exposure to three environmentally relevant PFAS compounds | PRJNA1011844 | Other | The per and polyfluoroalkyl substances PFAS are of significant global concern due to their highly ubiquitous and persistent nature bioaccumulation in organisms and potential toxicity. The aquatic environment is known as an important sink for PFAS resulting in high concentrations in aquatic organisms. However little is known about the developmental windows of sensitivity in which the PFAS chemicals are biologically active in addition to the toxicity endpoints that best reflect chemical hazard. In this study zebrafish Danio rerio were exposed to a 0.33% DMSO vehicle control 1uM chlorpyrifos CAS 2921 88 2 positive control and eight concentrations 0 100 uM half log dilutions of three environmentally relevant PFAS compounds in concentration response: PFOS CAS 1763 21 1 PFOA CAS 45285 51 6 and PFHxS CAS 355 46 4. There was also a group of unexposed zebrafish aliquoted from a single pool into all exposure plates to serve as a quality assurance measure. The goal of this study was to generate transcriptomic point of departure tPOD; a benchmark dose/concentration based treatment level below which a concerted gene expression response is not observed estimates for zebrafish exposed to PFAS compounds as a health protective exposure level for risk assessment. Through the use of short term embryo/larval plate based high throughput toxicity tests tPODs were determined across seven distinct developmental windows 6 hpf 24 hpf 6 hpf 48 hpf 24 hpf 48 hpf 6 hpf 120 hpf 24 hpf 120 hpf 48 hpf 120 hpf 96 hpf 120 hpf to assess how common experimental design variables e.g. different exposure durations exposure at different developmental stages affect point of departure estimates. | T7Ce | strain:AB wild type|age:96 120hpf|dev stage:embryo|collection date:2022|geo loc name:USA: Minnesota Duluth|sex:not applicable|tissue:whole body zebrafish embryo|biomaterial provider:US EPA Great Lakes Toxicology & Ecology Division 6201 Congdon Blvd Duluth MN 56809|breeding method:Adult zebrafish AB wild type strain were housed in an onsite culture facility at the US Environmental Protection Agency USEPA laboratory in Duluth MN. The fish were raised in a flow through system with control UV treated filtered Lake Superior water LSW at a flow rate of 250 mL/minute. Fish were held at 26 ± 1°C under a 16/8 hour light/dark photoperiod cycle. Fish were housed in 5.5 gallon tanks with <100 zebrafish per tank. Adult fish were fed live brine shrimp Artemia nauplii twice daily. The night prior breeding zebrafish in groups of 4 males x 6 females were separated into breeding tanks containing a plastic screened spawning basket. The next morning approximately 2 hours post the lights turned on embryos were collected and maintained in filtered LSW in an incubator set at 28.5°C. At approximately 4 hpf zebrafish embryos were screened under a stereo microscope and only similarly staged embryos were sorted out for chemical exposure. All dead malformed and unfertilized eggs were discarded.|collected by:Great Lakes Toxicology & Ecology Division|sample type:Total RNA|time code:7|dose:350.59|dose units:ug/L|treatment:PC transcr Chlorpyrifos CAS 2921 88 2|replicate ID:rep3|repeat sample:No|BioSampleModel:Model organism or animal | RNA Seq of danio rerio: whole organism embryo positive control Chlorpyrifos CAS 2921 88 2 | T7Ce S85 | T7Ce S85 | At the end of each PFAS exposure period zebrafih embryos were homogenized in Qiagen buffer RLT and betamercaptoethanol then frozen. RNA was isolated with Ambion MagMAX 96 Total RNA Isolation kit. Samples were transferred to 0.5 mL Eppendorf tubes in prepration for RNA Seq library prepation. RNA was normalized to 6 ng/uL using epMotion 5075. Illumina compatible Lexogen CORALL RNA Seq libraries were then prepared for RNA sequencing. Library pools were quality checked and quantified using a combination of Qubit dsDNA HS Agilent 4200 TapeStation HS DNA1000 and Invitrogen Collibri Library Quantification qPCR assays by the Michigan State University RTSF Genomics Core. Each pool was loaded onto 1 lane of a NovaSeq S4 flow cell. Sequencing was performed by Michigan State University in a 2x150bp paired end format using a NovaSeq 6000 v1.5 300 cycle reagent kit. Base calling was done by Illumina Real Time Analysis RTA v3.4.4 and output of RTA was demultiplexed and converted to FastQ format with Illumina Bcl2fastq v2.20.0. | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457982 | T7Ce_S85_L003_R1_001.fastq.gz T7Ce_S85_L003_R2_001.fastq.gz | fastq fastq | 4023236400.0 | 13410788.0 | T7Ce S85 L003 R1 001.fastq.gz | 0:150 1:150 | A:1064722362;C:898468046;G:1026541856;T:1033441788;N:62348 | 150 | 150 | 1064722362 | 898468046 | 1026541856 | 1033441788 | 62348 | SRX21590526 | SRS18768099 | SRA1703741 | U.S. Environmental Protection Agency|Great Lakes Toxicology and Ecology Division | U.S. Environmental Protection Agency | 2 | 0.63998 | 0.64782 | 0.1145 | 0.11833 | 0.72476 | 0.72366 | 0.51386 | 0.50933 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | random_priming | lexogen | bulk | unknown | unknown | United States | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 25370 | 25370 | SRR25869115 | SRX21590525 | SRS18768098 | SRP457982 | PRJNA1011844 | Comparison of zebrafish toxicity among different developmental windows of exposure to three environmentally relevant PFAS compounds | PRJNA1011844 | Other | The per and polyfluoroalkyl substances PFAS are of significant global concern due to their highly ubiquitous and persistent nature bioaccumulation in organisms and potential toxicity. The aquatic environment is known as an important sink for PFAS resulting in high concentrations in aquatic organisms. However little is known about the developmental windows of sensitivity in which the PFAS chemicals are biologically active in addition to the toxicity endpoints that best reflect chemical hazard. In this study zebrafish Danio rerio were exposed to a 0.33% DMSO vehicle control 1uM chlorpyrifos CAS 2921 88 2 positive control and eight concentrations 0 100 uM half log dilutions of three environmentally relevant PFAS compounds in concentration response: PFOS CAS 1763 21 1 PFOA CAS 45285 51 6 and PFHxS CAS 355 46 4. There was also a group of unexposed zebrafish aliquoted from a single pool into all exposure plates to serve as a quality assurance measure. The goal of this study was to generate transcriptomic point of departure tPOD; a benchmark dose/concentration based treatment level below which a concerted gene expression response is not observed estimates for zebrafish exposed to PFAS compounds as a health protective exposure level for risk assessment. Through the use of short term embryo/larval plate based high throughput toxicity tests tPODs were determined across seven distinct developmental windows 6 hpf 24 hpf 6 hpf 48 hpf 24 hpf 48 hpf 6 hpf 120 hpf 24 hpf 120 hpf 48 hpf 120 hpf 96 hpf 120 hpf to assess how common experimental design variables e.g. different exposure durations exposure at different developmental stages affect point of departure estimates. | T7Cd | strain:AB wild type|age:96 120hpf|dev stage:embryo|collection date:2022|geo loc name:USA: Minnesota Duluth|sex:not applicable|tissue:whole body zebrafish embryo|biomaterial provider:US EPA Great Lakes Toxicology & Ecology Division 6201 Congdon Blvd Duluth MN 56808|breeding method:Adult zebrafish AB wild type strain were housed in an onsite culture facility at the US Environmental Protection Agency USEPA laboratory in Duluth MN. The fish were raised in a flow through system with control UV treated filtered Lake Superior water LSW at a flow rate of 250 mL/minute. Fish were held at 26 ± 1°C under a 16/8 hour light/dark photoperiod cycle. Fish were housed in 5.5 gallon tanks with <100 zebrafish per tank. Adult fish were fed live brine shrimp Artemia nauplii twice daily. The night prior breeding zebrafish in groups of 4 males x 6 females were separated into breeding tanks containing a plastic screened spawning basket. The next morning approximately 2 hours post the lights turned on embryos were collected and maintained in filtered LSW in an incubator set at 28.5°C. At approximately 4 hpf zebrafish embryos were screened under a stereo microscope and only similarly staged embryos were sorted out for chemical exposure. All dead malformed and unfertilized eggs were discarded.|collected by:Great Lakes Toxicology & Ecology Division|sample type:Total RNA|time code:7|dose:350.59|dose units:ug/L|treatment:PC transcr Chlorpyrifos CAS 2921 88 2|replicate ID:rep2|repeat sample:No|BioSampleModel:Model organism or animal | RNA Seq of danio rerio: whole organism embryo positive control Chlorpyrifos CAS 2921 88 2 | T7Cd S9 | T7Cd S9 | At the end of each PFAS exposure period zebrafih embryos were homogenized in Qiagen buffer RLT and betamercaptoethanol then frozen. RNA was isolated with Ambion MagMAX 96 Total RNA Isolation kit. Samples were transferred to 0.5 mL Eppendorf tubes in prepration for RNA Seq library prepation. RNA was normalized to 6 ng/uL using epMotion 5075. Illumina compatible Lexogen CORALL RNA Seq libraries were then prepared for RNA sequencing. Library pools were quality checked and quantified using a combination of Qubit dsDNA HS Agilent 4200 TapeStation HS DNA1000 and Invitrogen Collibri Library Quantification qPCR assays by the Michigan State University RTSF Genomics Core. Each pool was loaded onto 1 lane of a NovaSeq S4 flow cell. Sequencing was performed by Michigan State University in a 2x150bp paired end format using a NovaSeq 6000 v1.5 300 cycle reagent kit. Base calling was done by Illumina Real Time Analysis RTA v3.4.4 and output of RTA was demultiplexed and converted to FastQ format with Illumina Bcl2fastq v2.20.0. | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457982 | T7Cd_S9_L003_R1_001.fastq.gz T7Cd_S9_L003_R2_001.fastq.gz | fastq fastq | 5594836800.0 | 18649456.0 | T7Cd S9 L003 R1 001.fastq.gz | 0:150 1:150 | A:1466668075;C:1268623063;G:1444679585;T:1414780182;N:85895 | 150 | 150 | 1466668075 | 1268623063 | 1444679585 | 1414780182 | 85895 | SRX21590525 | SRS18768098 | SRA1703741 | U.S. Environmental Protection Agency|Great Lakes Toxicology and Ecology Division | U.S. Environmental Protection Agency | 2 | 0.6489 | 0.65814 | 0.10603 | 0.1096 | 0.72332 | 0.72259 | 0.51745 | 0.51597 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | random_priming | lexogen | bulk | unknown | unknown | United States | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 25371 | 25371 | SRR25869116 | SRX21590524 | SRS18768097 | SRP457982 | PRJNA1011844 | Comparison of zebrafish toxicity among different developmental windows of exposure to three environmentally relevant PFAS compounds | PRJNA1011844 | Other | The per and polyfluoroalkyl substances PFAS are of significant global concern due to their highly ubiquitous and persistent nature bioaccumulation in organisms and potential toxicity. The aquatic environment is known as an important sink for PFAS resulting in high concentrations in aquatic organisms. However little is known about the developmental windows of sensitivity in which the PFAS chemicals are biologically active in addition to the toxicity endpoints that best reflect chemical hazard. In this study zebrafish Danio rerio were exposed to a 0.33% DMSO vehicle control 1uM chlorpyrifos CAS 2921 88 2 positive control and eight concentrations 0 100 uM half log dilutions of three environmentally relevant PFAS compounds in concentration response: PFOS CAS 1763 21 1 PFOA CAS 45285 51 6 and PFHxS CAS 355 46 4. There was also a group of unexposed zebrafish aliquoted from a single pool into all exposure plates to serve as a quality assurance measure. The goal of this study was to generate transcriptomic point of departure tPOD; a benchmark dose/concentration based treatment level below which a concerted gene expression response is not observed estimates for zebrafish exposed to PFAS compounds as a health protective exposure level for risk assessment. Through the use of short term embryo/larval plate based high throughput toxicity tests tPODs were determined across seven distinct developmental windows 6 hpf 24 hpf 6 hpf 48 hpf 24 hpf 48 hpf 6 hpf 120 hpf 24 hpf 120 hpf 48 hpf 120 hpf 96 hpf 120 hpf to assess how common experimental design variables e.g. different exposure durations exposure at different developmental stages affect point of departure estimates. | T7Cc | strain:AB wild type|age:96 120hpf|dev stage:embryo|collection date:2022|geo loc name:USA: Minnesota Duluth|sex:not applicable|tissue:whole body zebrafish embryo|biomaterial provider:US EPA Great Lakes Toxicology & Ecology Division 6201 Congdon Blvd Duluth MN 56807|breeding method:Adult zebrafish AB wild type strain were housed in an onsite culture facility at the US Environmental Protection Agency USEPA laboratory in Duluth MN. The fish were raised in a flow through system with control UV treated filtered Lake Superior water LSW at a flow rate of 250 mL/minute. Fish were held at 26 ± 1°C under a 16/8 hour light/dark photoperiod cycle. Fish were housed in 5.5 gallon tanks with <100 zebrafish per tank. Adult fish were fed live brine shrimp Artemia nauplii twice daily. The night prior breeding zebrafish in groups of 4 males x 6 females were separated into breeding tanks containing a plastic screened spawning basket. The next morning approximately 2 hours post the lights turned on embryos were collected and maintained in filtered LSW in an incubator set at 28.5°C. At approximately 4 hpf zebrafish embryos were screened under a stereo microscope and only similarly staged embryos were sorted out for chemical exposure. All dead malformed and unfertilized eggs were discarded.|collected by:Great Lakes Toxicology & Ecology Division|sample type:Total RNA|time code:7|dose:350.59|dose units:ug/L|treatment:PC transcr Chlorpyrifos CAS 2921 88 2|replicate ID:rep1|repeat sample:No|BioSampleModel:Model organism or animal | RNA Seq of danio rerio: whole organism embryo positive control Chlorpyrifos CAS 2921 88 2 | T7Cc S117 | T7Cc S117 | At the end of each PFAS exposure period zebrafih embryos were homogenized in Qiagen buffer RLT and betamercaptoethanol then frozen. RNA was isolated with Ambion MagMAX 96 Total RNA Isolation kit. Samples were transferred to 0.5 mL Eppendorf tubes in prepration for RNA Seq library prepation. RNA was normalized to 6 ng/uL using epMotion 5075. Illumina compatible Lexogen CORALL RNA Seq libraries were then prepared for RNA sequencing. Library pools were quality checked and quantified using a combination of Qubit dsDNA HS Agilent 4200 TapeStation HS DNA1000 and Invitrogen Collibri Library Quantification qPCR assays by the Michigan State University RTSF Genomics Core. Each pool was loaded onto 1 lane of a NovaSeq S4 flow cell. Sequencing was performed by Michigan State University in a 2x150bp paired end format using a NovaSeq 6000 v1.5 300 cycle reagent kit. Base calling was done by Illumina Real Time Analysis RTA v3.4.4 and output of RTA was demultiplexed and converted to FastQ format with Illumina Bcl2fastq v2.20.0. | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457982 | T7Cc_S117_L003_R1_001.fastq.gz T7Cc_S117_L003_R2_001.fastq.gz | fastq fastq | 5560971900.0 | 18536573.0 | T7Cc S117 L003 R1 001.fastq.gz | 0:150 1:150 | A:1487669019;C:1227367015;G:1414625121;T:1431224819;N:85926 | 150 | 150 | 1487669019 | 1227367015 | 1414625121 | 1431224819 | 85926 | SRX21590524 | SRS18768097 | SRA1703741 | U.S. Environmental Protection Agency|Great Lakes Toxicology and Ecology Division | U.S. Environmental Protection Agency | 2 | 0.63573 | 0.6453 | 0.11688 | 0.12088 | 0.72997 | 0.72902 | 0.51338 | 0.51387 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | random_priming | lexogen | bulk | unknown | unknown | United States | 2023-09-01 | Larval | Larval | Trunk | Surface Structure | |||||||||||||||||||||
| 25372 | 25372 | SRR25869117 | SRX21590523 | SRS18768096 | SRP457982 | PRJNA1011844 | Comparison of zebrafish toxicity among different developmental windows of exposure to three environmentally relevant PFAS compounds | PRJNA1011844 | Other | The per and polyfluoroalkyl substances PFAS are of significant global concern due to their highly ubiquitous and persistent nature bioaccumulation in organisms and potential toxicity. The aquatic environment is known as an important sink for PFAS resulting in high concentrations in aquatic organisms. However little is known about the developmental windows of sensitivity in which the PFAS chemicals are biologically active in addition to the toxicity endpoints that best reflect chemical hazard. In this study zebrafish Danio rerio were exposed to a 0.33% DMSO vehicle control 1uM chlorpyrifos CAS 2921 88 2 positive control and eight concentrations 0 100 uM half log dilutions of three environmentally relevant PFAS compounds in concentration response: PFOS CAS 1763 21 1 PFOA CAS 45285 51 6 and PFHxS CAS 355 46 4. There was also a group of unexposed zebrafish aliquoted from a single pool into all exposure plates to serve as a quality assurance measure. The goal of this study was to generate transcriptomic point of departure tPOD; a benchmark dose/concentration based treatment level below which a concerted gene expression response is not observed estimates for zebrafish exposed to PFAS compounds as a health protective exposure level for risk assessment. Through the use of short term embryo/larval plate based high throughput toxicity tests tPODs were determined across seven distinct developmental windows 6 hpf 24 hpf 6 hpf 48 hpf 24 hpf 48 hpf 6 hpf 120 hpf 24 hpf 120 hpf 48 hpf 120 hpf 96 hpf 120 hpf to assess how common experimental design variables e.g. different exposure durations exposure at different developmental stages affect point of departure estimates. | T6Ce | strain:AB wild type|age:48 120hpf|dev stage:embryo|collection date:2022|geo loc name:USA: Minnesota Duluth|sex:not applicable|tissue:whole body zebrafish embryo|biomaterial provider:US EPA Great Lakes Toxicology & Ecology Division 6201 Congdon Blvd Duluth MN 56806|breeding method:Adult zebrafish AB wild type strain were housed in an onsite culture facility at the US Environmental Protection Agency USEPA laboratory in Duluth MN. The fish were raised in a flow through system with control UV treated filtered Lake Superior water LSW at a flow rate of 250 mL/minute. Fish were held at 26 ± 1°C under a 16/8 hour light/dark photoperiod cycle. Fish were housed in 5.5 gallon tanks with <100 zebrafish per tank. Adult fish were fed live brine shrimp Artemia nauplii twice daily. The night prior breeding zebrafish in groups of 4 males x 6 females were separated into breeding tanks containing a plastic screened spawning basket. The next morning approximately 2 hours post the lights turned on embryos were collected and maintained in filtered LSW in an incubator set at 28.5°C. At approximately 4 hpf zebrafish embryos were screened under a stereo microscope and only similarly staged embryos were sorted out for chemical exposure. All dead malformed and unfertilized eggs were discarded.|collected by:Great Lakes Toxicology & Ecology Division|sample type:Total RNA|time code:6|dose:350.59|dose units:ug/L|treatment:PC transcr Chlorpyrifos CAS 2921 88 2|replicate ID:rep3|repeat sample:No|BioSampleModel:Model organism or animal | RNA Seq of danio rerio: whole organism embryo positive control Chlorpyrifos CAS 2921 88 2 | T6Ce S8 | T6Ce S8 | At the end of each PFAS exposure period zebrafih embryos were homogenized in Qiagen buffer RLT and betamercaptoethanol then frozen. RNA was isolated with Ambion MagMAX 96 Total RNA Isolation kit. Samples were transferred to 0.5 mL Eppendorf tubes in prepration for RNA Seq library prepation. RNA was normalized to 6 ng/uL using epMotion 5075. Illumina compatible Lexogen CORALL RNA Seq libraries were then prepared for RNA sequencing. Library pools were quality checked and quantified using a combination of Qubit dsDNA HS Agilent 4200 TapeStation HS DNA1000 and Invitrogen Collibri Library Quantification qPCR assays by the Michigan State University RTSF Genomics Core. Each pool was loaded onto 1 lane of a NovaSeq S4 flow cell. Sequencing was performed by Michigan State University in a 2x150bp paired end format using a NovaSeq 6000 v1.5 300 cycle reagent kit. Base calling was done by Illumina Real Time Analysis RTA v3.4.4 and output of RTA was demultiplexed and converted to FastQ format with Illumina Bcl2fastq v2.20.0. | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina NovaSeq 6000 | SRP457982 | T6Ce_S8_L003_R1_001.fastq.gz T6Ce_S8_L003_R2_001.fastq.gz | fastq fastq | 4874754000.0 | 16249180.0 | T6Ce S8 L003 R1 001.fastq.gz | 0:150 1:150 | A:1274050261;C:1103676303;G:1253372135;T:1243579950;N:75351 | 150 | 150 | 1274050261 | 1103676303 | 1253372135 | 1243579950 | 75351 | SRX21590523 | SRS18768096 | SRA1703741 | U.S. Environmental Protection Agency|Great Lakes Toxicology and Ecology Division | U.S. Environmental Protection Agency | 2 | 0.63046 | 0.63966 | 0.07875 | 0.08075 | 0.71681 | 0.71549 | 0.47414 | 0.46325 | 150 | 150 | B | B | biological fallback assumption | illumina | novaseq_era | unknown | random_priming | lexogen | bulk | unknown | unknown | United States | 2023-09-01 | Larval | Larval | Trunk | Surface Structure |
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CREATE TABLE run_metadata("run.accession" VARCHAR, "experiment.accession" VARCHAR, "sample.accession" VARCHAR, "study.accession" VARCHAR, bioproject VARCHAR, "study.title" VARCHAR, "study.alias" VARCHAR, "study.type" VARCHAR, "study.abstract" VARCHAR, "study.attributes" VARCHAR, "study.PMIDs" VARCHAR, "sample.description" VARCHAR, "sample.title" VARCHAR, "sample.alias" VARCHAR, "sample.centername" VARCHAR, "sample.attributes" VARCHAR, "GEOsample.title" VARCHAR, "GEOsample.dataprocessing" VARCHAR, "GEOsample.source" VARCHAR, "GEOsample.treatmentprotocol" VARCHAR, "GEOsample.extractprotocol" VARCHAR, "GEOsample.growthprotocol" VARCHAR, "GEOsample.characteristics" VARCHAR, "GEOsample.accession" VARCHAR, "experiment.title" VARCHAR, "experiment.alias" VARCHAR, "experiment.library_name" VARCHAR, "experiment.design_description" VARCHAR, "experiment.library_construction_protocol" VARCHAR, "experiment.attributes" VARCHAR, "experiment.library_strategy" VARCHAR, "experiment.library_source" VARCHAR, "experiment.library_selection" VARCHAR, "experiment.library_layout" VARCHAR, "experiment.platform" VARCHAR, "experiment.instrument_model" VARCHAR, "experiment.spot_descriptor" VARCHAR, "experiment.study_ref" VARCHAR, "run.title" VARCHAR, "run.attributes" VARCHAR, "run.filename" VARCHAR, "run.semantic_name" VARCHAR, "run.total_bases" DOUBLE, "run.total_spots" DOUBLE, "run.alias" VARCHAR, "run.read_lengths" VARCHAR, "run.base_counts" VARCHAR, "run.r1_length" BIGINT, "run.r2_length" BIGINT, "run.r3_length" BIGINT, "run.r4_length" BIGINT, "run.Acount" BIGINT, "run.Ccount" BIGINT, "run.Gcount" BIGINT, "run.Tcount" BIGINT, "run.Ncount" BIGINT, "run.experiment" VARCHAR, "run.pool_member" VARCHAR, "submission.accession" VARCHAR, "submission.srasource" VARCHAR, "submission.bioprojectsource" VARCHAR, "seqdetective.n_mates" BIGINT, "seqdetective.mapping_rate.mate1" DOUBLE, "seqdetective.mapping_rate.mate2" DOUBLE, "seqdetective.nofeature_rate.mate1" DOUBLE, "seqdetective.nofeature_rate.mate2" DOUBLE, "seqdetective.sparsity.mate1" DOUBLE, "seqdetective.sparsity.mate2" DOUBLE, "seqdetective.pos_strand_rate.mate1" DOUBLE, "seqdetective.pos_strand_rate.mate2" DOUBLE, "seqdetective.readlen.mate1" BIGINT, "seqdetective.readlen.mate2" BIGINT, "seqdetective.judgement.mate1" VARCHAR, "seqdetective.judgement.mate2" VARCHAR, "seqdetective.judgement.reason" VARCHAR, platform_family VARCHAR, instrument_generation VARCHAR, read_bias VARCHAR, selection_class VARCHAR, prep_kit VARCHAR, sc_or_bulk VARCHAR, tech_class VARCHAR, technology VARCHAR, tech_variant VARCHAR, "submission.bioprojectsource.country" VARCHAR, earliest_date DATE, devstage_curation VARCHAR, devstage_curation_coarse VARCHAR, tissue_curation VARCHAR, tissue_curation_coarse VARCHAR);;
CREATE INDEX idx_run_bioproject ON run_metadata(bioproject);;
CREATE INDEX idx_run_run_accession ON run_metadata("run.accession");;