run_metadata
25 rows where experiment.library_layout = "SINGLE", experiment.library_selection = "Oligo-dT" and tissue_curation_coarse = "Reproductive System"
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| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 29259 | 29259 | SRR27336917 | SRX23013778 | SRS19977075 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalKO gonads 31dpf rep2 | miR214 PaternalKO gonads 31dpf rep2 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalKO|biological replicate:rep2|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A11 | miR214 PaternalKO gonads 31dpf rep2 | miR214 PaternalKO gonads 31dpf rep2 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalKO_gonads_31dpf_rep2.fastq.gz | fastq | 2327996832.0 | 27714248.0 | miR214 PaternalKO gonads 31dpf rep2.fastq.gz | 0:84 | A:602135965;C:552786494;G:537368428;T:635697339;N:8606 | 84 | 602135965 | 552786494 | 537368428 | 635697339 | 8606 | SRX23013778 | SRS19977075 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95369 | 0.06146 | 0.69203 | 0.47259 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29260 | 29260 | SRR27336918 | SRX23013777 | SRS19977074 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalKO gonads 31dpf rep1 | miR214 PaternalKO gonads 31dpf rep1 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalKO|biological replicate:rep1|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A10 | miR214 PaternalKO gonads 31dpf rep1 | miR214 PaternalKO gonads 31dpf rep1 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalKO_gonads_31dpf_rep1.fastq.gz | fastq | 2500978452.0 | 29773553.0 | miR214 PaternalKO gonads 31dpf rep1.fastq.gz | 0:84 | A:646162933;C:593855971;G:578265372;T:682684551;N:9625 | 84 | 646162933 | 593855971 | 578265372 | 682684551 | 9625 | SRX23013777 | SRS19977074 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95147 | 0.05972 | 0.69071 | 0.47043 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29261 | 29261 | SRR27336919 | SRX23013776 | SRS19977073 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalHET gonads 31dpf rep4 | miR214 maternalHET gonads 31dpf rep4 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalHET|biological replicate:rep4|number of gonads:7 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A9 | miR214 maternalHET gonads 31dpf rep4 | miR214 maternalHET gonads 31dpf rep4 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalHET_gonads_31dpf_rep4.fastq.gz | fastq | 2365480908.0 | 28160487.0 | miR214 maternalHET gonads 31dpf rep4.fastq.gz | 0:84 | A:613121312;C:560582165;G:549338096;T:642429834;N:9501 | 84 | 613121312 | 560582165 | 549338096 | 642429834 | 9501 | SRX23013776 | SRS19977073 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95304 | 0.05342 | 0.7108 | 0.46822 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29262 | 29262 | SRR27336920 | SRX23013775 | SRS19977072 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalHET gonads 31dpf rep3 | miR214 maternalHET gonads 31dpf rep3 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalHET|biological replicate:rep3|number of gonads:7 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A8 | miR214 maternalHET gonads 31dpf rep3 | miR214 maternalHET gonads 31dpf rep3 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalHET_gonads_31dpf_rep3.fastq.gz | fastq | 2537794644.0 | 30211841.0 | miR214 maternalHET gonads 31dpf rep3.fastq.gz | 0:84 | A:658687178;C:600742464;G:585643169;T:692712057;N:9776 | 84 | 658687178 | 600742464 | 585643169 | 692712057 | 9776 | SRX23013775 | SRS19977072 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95177 | 0.06701 | 0.68195 | 0.47393 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29263 | 29263 | SRR27336921 | SRX23013774 | SRS19977071 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalHET gonads 31dpf rep2 | miR214 maternalHET gonads 31dpf rep2 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalHET|biological replicate:rep2|number of gonads:7 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A7 | miR214 maternalHET gonads 31dpf rep2 | miR214 maternalHET gonads 31dpf rep2 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalHET_gonads_31dpf_rep2.fastq.gz | fastq | 2417384424.0 | 28778386.0 | miR214 maternalHET gonads 31dpf rep2.fastq.gz | 0:84 | A:625935186;C:574179061;G:560498085;T:656762980;N:9112 | 84 | 625935186 | 574179061 | 560498085 | 656762980 | 9112 | SRX23013774 | SRS19977071 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95259 | 0.05852 | 0.6981 | 0.47435 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29264 | 29264 | SRR27336922 | SRX23013773 | SRS19977070 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalHET gonads 31dpf rep1 | miR214 maternalHET gonads 31dpf rep1 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalHET|biological replicate:rep1|number of gonads:7 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A6 | miR214 maternalHET gonads 31dpf rep1 | miR214 maternalHET gonads 31dpf rep1 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalHET_gonads_31dpf_rep1.fastq.gz | fastq | 2330886180.0 | 27748645.0 | miR214 maternalHET gonads 31dpf rep1.fastq.gz | 0:84 | A:601589571;C:554105326;G:542789267;T:632393158;N:8858 | 84 | 601589571 | 554105326 | 542789267 | 632393158 | 8858 | SRX23013773 | SRS19977070 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95338 | 0.05239 | 0.71366 | 0.47291 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29265 | 29265 | SRR27336923 | SRX23013772 | SRS19977069 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalKO gonads 31dpf rep4 | miR214 maternalKO gonads 31dpf rep4 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalKO|biological replicate:rep4|number of gonads:8 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A5 | miR214 maternalKO gonads 31dpf rep4 | miR214 maternalKO gonads 31dpf rep4 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalKO_gonads_31dpf_rep4.fastq.gz | fastq | 2340233784.0 | 27859926.0 | miR214 maternalKO gonads 31dpf rep4.fastq.gz | 0:84 | A:606735187;C:553647808;G:539865459;T:639976430;N:8900 | 84 | 606735187 | 553647808 | 539865459 | 639976430 | 8900 | SRX23013772 | SRS19977069 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95406 | 0.06415 | 0.68225 | 0.47695 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29266 | 29266 | SRR27336924 | SRX23013771 | SRS19977068 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalKO gonads 31dpf rep3 | miR214 maternalKO gonads 31dpf rep3 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalKO|biological replicate:rep3|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A4 | miR214 maternalKO gonads 31dpf rep3 | miR214 maternalKO gonads 31dpf rep3 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalKO_gonads_31dpf_rep3.fastq.gz | fastq | 2058505512.0 | 24506018.0 | miR214 maternalKO gonads 31dpf rep3.fastq.gz | 0:84 | A:537425814;C:485664494;G:471526682;T:563881213;N:7309 | 84 | 537425814 | 485664494 | 471526682 | 563881213 | 7309 | SRX23013771 | SRS19977068 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95296 | 0.06728 | 0.69266 | 0.47627 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29267 | 29267 | SRR27336925 | SRX23013770 | SRS19977067 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalHET gonads 31dpf rep4 | miR214 PaternalHET gonads 31dpf rep4 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalHET|biological replicate:rep4|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A17 | miR214 PaternalHET gonads 31dpf rep4 | miR214 PaternalHET gonads 31dpf rep4 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalHET_gonads_31dpf_rep4.fastq.gz | fastq | 3001613328.0 | 35733492.0 | miR214 PaternalHET gonads 31dpf rep4.fastq.gz | 0:84 | A:778860501;C:711155422;G:688784969;T:822801157;N:11279 | 84 | 778860501 | 711155422 | 688784969 | 822801157 | 11279 | SRX23013770 | SRS19977067 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95361 | 0.05653 | 0.7051 | 0.48382 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29268 | 29268 | SRR27336926 | SRX23013769 | SRS19977066 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalHET gonads 31dpf rep3 | miR214 PaternalHET gonads 31dpf rep3 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalHET|biological replicate:rep3|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A16 | miR214 PaternalHET gonads 31dpf rep3 | miR214 PaternalHET gonads 31dpf rep3 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalHET_gonads_31dpf_rep3.fastq.gz | fastq | 3053630664.0 | 36352746.0 | miR214 PaternalHET gonads 31dpf rep3.fastq.gz | 0:84 | A:785219727;C:726431662;G:713454025;T:828513556;N:11694 | 84 | 785219727 | 726431662 | 713454025 | 828513556 | 11694 | SRX23013769 | SRS19977066 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95309 | 0.04588 | 0.71997 | 0.46447 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29269 | 29269 | SRR27336927 | SRX23013768 | SRS19977065 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalHET gonads 31dpf rep2 | miR214 PaternalHET gonads 31dpf rep2 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalHET|biological replicate:rep2|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A15 | miR214 PaternalHET gonads 31dpf rep2 | miR214 PaternalHET gonads 31dpf rep2 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalHET_gonads_31dpf_rep2.fastq.gz | fastq | 3063695208.0 | 36472562.0 | miR214 PaternalHET gonads 31dpf rep2.fastq.gz | 0:84 | A:784924646;C:728941687;G:720847462;T:828969510;N:11903 | 84 | 784924646 | 728941687 | 720847462 | 828969510 | 11903 | SRX23013768 | SRS19977065 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95413 | 0.04739 | 0.71936 | 0.4704 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29270 | 29270 | SRR27336928 | SRX23013767 | SRS19977064 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalHET gonads 31dpf rep1 | miR214 PaternalHET gonads 31dpf rep1 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalHET|biological replicate:rep1|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:heterozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A14 | miR214 PaternalHET gonads 31dpf rep1 | miR214 PaternalHET gonads 31dpf rep1 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalHET_gonads_31dpf_rep1.fastq.gz | fastq | 2699154024.0 | 32132786.0 | miR214 PaternalHET gonads 31dpf rep1.fastq.gz | 0:84 | A:694174797;C:642049572;G:627991562;T:734927762;N:10331 | 84 | 694174797 | 642049572 | 627991562 | 734927762 | 10331 | SRX23013767 | SRS19977064 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95518 | 0.05525 | 0.70285 | 0.47695 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29271 | 29271 | SRR27336929 | SRX23013766 | SRS19977063 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalKO gonads 31dpf rep4 | miR214 PaternalKO gonads 31dpf rep4 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalKO|biological replicate:rep4|number of gonads:8 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A13 | miR214 PaternalKO gonads 31dpf rep4 | miR214 PaternalKO gonads 31dpf rep4 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalKO_gonads_31dpf_rep4.fastq.gz | fastq | 2514248016.0 | 29931524.0 | miR214 PaternalKO gonads 31dpf rep4.fastq.gz | 0:84 | A:648908956;C:598837726;G:580002743;T:686488678;N:9913 | 84 | 648908956 | 598837726 | 580002743 | 686488678 | 9913 | SRX23013766 | SRS19977063 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.94978 | 0.06951 | 0.67896 | 0.47686 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29272 | 29272 | SRR27336930 | SRX23013765 | SRS19977062 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 PaternalKO gonads 31dpf rep3 | miR214 PaternalKO gonads 31dpf rep3 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:PaternalKO|biological replicate:rep3|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a heterozygous female crossed to a homozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A12 | miR214 PaternalKO gonads 31dpf rep3 | miR214 PaternalKO gonads 31dpf rep3 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_PaternalKO_gonads_31dpf_rep3.fastq.gz | fastq | 2499529200.0 | 29756300.0 | miR214 PaternalKO gonads 31dpf rep3.fastq.gz | 0:84 | A:642490769;C:597403823;G:580565141;T:679060154;N:9313 | 84 | 642490769 | 597403823 | 580565141 | 679060154 | 9313 | SRX23013765 | SRS19977062 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95284 | 0.05602 | 0.70289 | 0.47154 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29273 | 29273 | SRR27336931 | SRX23013764 | SRS19977061 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalKO gonads 31dpf rep2 | miR214 maternalKO gonads 31dpf rep2 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalKO|biological replicate:rep2|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A3 | miR214 maternalKO gonads 31dpf rep2 | miR214 maternalKO gonads 31dpf rep2 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalKO_gonads_31dpf_rep2.fastq.gz | fastq | 2529742404.0 | 30115981.0 | miR214 maternalKO gonads 31dpf rep2.fastq.gz | 0:84 | A:652091166;C:600932059;G:589100617;T:687608862;N:9700 | 84 | 652091166 | 600932059 | 589100617 | 687608862 | 9700 | SRX23013764 | SRS19977061 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95498 | 0.05524 | 0.70366 | 0.47319 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29274 | 29274 | SRR27336932 | SRX23013763 | SRS19977060 | SRP479907 | PRJNA1056454 | miR214 regulates sex determination through gsdf in zebrafish | PRJNA1056454 | Other | Sex determination is a variable and complex mechanism yet it can be found all over the plant and animal kingdoms. It creates two morphological different outcomes from one and the same species. Our work demonstrates the involvement of a non coding RNA in this process for the teleost Danio rerio. Although we were not able to understand the full mechanism behind it we can provide a piece of the puzzle which once again highlights the complexity and flexibility of sex determination. | CrisprCas9 generated using 2 sgRNAs >F3 crossed toTgvasa:eGFP | miR214 maternalKO gonads 31dpf rep1 | miR214 maternalKO gonads 31dpf rep1 | strain:mz 06de tgvasa:eGFP|isolate:not applicable|breed:TUE|cultivar:not applicable|ecotype:not applicable|age:27 dpf|dev stage:27 dpf|sex:not applicable|tissue:gonads|parental ko:maternalKO|biological replicate:rep1|number of gonads:9 gonads|birth date:21.09.2018|collection date:not applicable|genotype:homozygous mutation for miR 214 from a homozygous female crossed to a heterozygous male|geo loc name:not applicable|growth protocol:standard|phenotype:n1|sample type:tissue|BioSampleModel:Model organism or animal | = xlfn.CONCAT"mrna sequencing of zebrafish: " A2 | miR214 maternalKO gonads 31dpf rep1 | miR214 maternalKO gonads 31dpf rep1 | NGS library prep was performed with Illumina's TruSeq stranded mRNA LT Sample Prep Kit following Illuminas standard protocol Part # 15031047 Rev E. Libraries were prepared with a starting amount of 193 ng and amplified in 13 PCR cycles Libraries were profiled in a DNA 1000 Chip on a 2100 Bioanalyzer Agilent technologies and quantified using the Qubit dsDNA HS Assay Kit in a Qubit 2 0 Fluorometer Life technologies. All 16 samples were pooled in equimolar ratio and sequenced on 1 NextSeq 500 Highoutput FC SR for 1 x 84 cycles plus 7 cycles for the index read. | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP479907 | miR214_maternalKO_gonads_31dpf_rep1.fastq.gz | fastq | 2310878136.0 | 27510454.0 | miR214 maternalKO gonads 31dpf rep1.fastq.gz | 0:84 | A:598541924;C:547875391;G:533137786;T:631314274;N:8761 | 84 | 598541924 | 547875391 | 533137786 | 631314274 | 8761 | SRX23013763 | SRS19977060 | SRA1775014 | Rene Ketting group|Ketting Lab | Rene Ketting group | 1 | 0.95279 | 0.06446 | 0.68757 | 0.4758 | 84 | B | usable mapping rate | illumina | nextseq | unknown | poly_a | trueseq | bulk | unknown | unknown | Germany | 2023-12-24 | Larval | Larval | Gonad | Reproductive System | ||||||||||||||||||||||||||
| 29720 | 29720 | SRR27485665 | SRX23156884 | SRS20107305 | SRP482074 | PRJNA1061456 | tRAM seq: tRNA abundance and modification analysis during zebrafish embryo development | PRJNA1061456 | Other | ovary R3 | strain:TLAB fish|isolate:NA|breed:cross of zebrafish AB and the natural variant TL Tupfel Longfin|cultivar:NA|ecotype:NA|dev stage:adult|collection date:2022|geo loc name:Austria|sex:female|tissue:ovary|replicate:3|BioSampleModel:Model organism or animal | mRNA seq of zebrafish: ovary rep4 | EV06008 | EV06008 | RNA was extracted with Trizol and processed with QuantSeq three prime mRNA Seq Library Prep Kit FWD for Illumina Lexogen. 500 ng total RNA per sample. Single indexed QuantSeq libraries were QC checked on a Bioanalyzer 2100 Agilent using a High Sensitivity DNA Kit for correct insert size and quantified using Qubit dsDNA HS Assay Invitrogen. Pooled libraries were sequenced on a NextSeq500 instrument Illumina in 1x75bp single end sequencing mode | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP482074 | EV06008.R1.fastq.gz | fastq | 585955025.0 | 7769646.0 | EV06008.R1.fastq.gz | 0:75.42 | A:167210227;C:106735220;G:128095616;T:183896888;N:17074 | 75 | 167210227 | 106735220 | 128095616 | 183896888 | 17074 | SRX23156884 | SRS20107305 | SRA1783314 | Medical University of Vienna|Cell and Developmental Biology | Medical University of Vienna | 1 | 0.85544 | 0.05096 | 0.78441 | 0.53007 | 76 | B | usable mapping rate | illumina | nextseq | 3prime | poly_a | lexogen | bulk | unknown | unknown | Austria | 2024-01-11 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||||
| 29731 | 29731 | SRR27485676 | SRX23156873 | SRS20107294 | SRP482074 | PRJNA1061456 | tRAM seq: tRNA abundance and modification analysis during zebrafish embryo development | PRJNA1061456 | Other | ovary R2 | strain:TLAB fish|isolate:NA|breed:cross of zebrafish AB and the natural variant TL Tupfel Longfin|cultivar:NA|ecotype:NA|dev stage:adult|collection date:2022|geo loc name:Austria|sex:female|tissue:ovary|replicate:2|BioSampleModel:Model organism or animal | mRNA seq of zebrafish: ovary rep4 | EV06001 | EV06001 | RNA was extracted with Trizol and processed with QuantSeq three prime mRNA Seq Library Prep Kit FWD for Illumina Lexogen. 500 ng total RNA per sample. Single indexed QuantSeq libraries were QC checked on a Bioanalyzer 2100 Agilent using a High Sensitivity DNA Kit for correct insert size and quantified using Qubit dsDNA HS Assay Invitrogen. Pooled libraries were sequenced on a NextSeq500 instrument Illumina in 1x75bp single end sequencing mode | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP482074 | EV06001.R1.fastq.gz | fastq | 685280356.0 | 9098789.0 | EV06001.R1.fastq.gz | 0:75.32 | A:194596366;C:122550539;G:153504013;T:214558450;N:70988 | 75 | 194596366 | 122550539 | 153504013 | 214558450 | 70988 | SRX23156873 | SRS20107294 | SRA1783314 | Medical University of Vienna|Cell and Developmental Biology | Medical University of Vienna | 1 | 0.8304 | 0.04498 | 0.80166 | 0.5028 | 74 | B | usable mapping rate | illumina | nextseq | 3prime | poly_a | lexogen | bulk | unknown | unknown | Austria | 2024-01-11 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||||
| 29738 | 29738 | SRR27477298 | SRX23148649 | SRS20099367 | SRP482074 | PRJNA1061456 | tRAM seq: tRNA abundance and modification analysis during zebrafish embryo development | PRJNA1061456 | Other | ovary R4 | strain:TLAB fish|isolate:NA|breed:cross of zebrafish AB and the natural variant TL Tupfel Longfin|cultivar:NA|ecotype:NA|dev stage:adult|collection date:2022|geo loc name:Austria|sex:female|tissue:ovary|replicate:4|BioSampleModel:Model organism or animal | mRNA seq of zebrafish: ovary rep4 | EV09001 | EV09001 | RNA was extracted with Trizol and processed with QuantSeq three prime mRNA Seq Library Prep Kit FWD for Illumina Lexogen. 500 ng total RNA per sample. Single indexed QuantSeq libraries were QC checked on a Bioanalyzer 2100 Agilent using a High Sensitivity DNA Kit for correct insert size and quantified using Qubit dsDNA HS Assay Invitrogen. Pooled libraries were sequenced on a NextSeq500 instrument Illumina in 1x75bp single end sequencing mode | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | NextSeq 500 | SRP482074 | EV09001.R1.fastq.gz | fastq | 456295310.0 | 6058854.0 | EV09001.R1.fastq.gz | 0:75.31 | A:135579999;C:83364677;G:101608151;T:135700843;N:41640 | 75 | 135579999 | 83364677 | 101608151 | 135700843 | 41640 | SRX23148649 | SRS20099367 | SRA1782413 | Medical University of Vienna|Cell and Developmental Biology | Medical University of Vienna | 1 | 0.85088 | 0.05876 | 0.7791 | 0.50948 | 75 | B | usable mapping rate | illumina | nextseq | 3prime | poly_a | lexogen | bulk | unknown | unknown | Austria | 2024-01-10 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||||
| 70364 | 70364 | SRR21073877 | SRX17088847 | SRS14371197 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | MT 6 | strain:AB|age:4 mpf of bmp4 deficient fish 3|BioSampleModel:Model organism or animal | RNAseq of follicle | s128 | s128 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | MT6.fq.gz | fastq | 3497983350.0 | 23319889.0 | MT6.fq.gz | 0:0 1:150 | A:925962113;C:824839459;G:828143623;T:919023343;N:14812 | 0 | 150 | 925962113 | 824839459 | 828143623 | 919023343 | 14812 | SRX17088847 | SRS14371197 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.94049 | 0.02767 | 0.72734 | 0.48914 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-16 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||
| 70365 | 70365 | SRR21073878 | SRX17088846 | SRS14371196 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | MT 5 | strain:AB|age:8 mpf of bmp4 deficient fish 2|BioSampleModel:Model organism or animal | RNAseq of follicle | s127 | s127 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | MT5.fq.gz | fastq | 3386696550.0 | 22577977.0 | MT5.fq.gz | 0:0 1:150 | A:912598403;C:783846328;G:783277440;T:906957617;N:16762 | 0 | 150 | 912598403 | 783846328 | 783277440 | 906957617 | 16762 | SRX17088846 | SRS14371196 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.9431 | 0.0445 | 0.71246 | 0.50398 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-16 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||
| 70366 | 70366 | SRR21073879 | SRX17088845 | SRS14371195 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | MT 4 | strain:AB|age:8 mpf of bmp4 deficient fish 1|BioSampleModel:Model organism or animal | RNAseq of follicle | s126 | s126 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | loader:fastq load.py | ._MT_4_2.fq MT_4_2.fq | fastq fastq | 1888773150.0 | 12591821.0 | MT4.fq.tar.gz | 0:150 | A:511378286;C:435985420;G:435316617;T:506079213;N:13614 | 150 | 511378286 | 435985420 | 435316617 | 506079213 | 13614 | SRX17088845 | SRS14371195 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.94333 | 0.04222 | 0.71478 | 0.50684 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-16 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||
| 70367 | 70367 | SRR21073880 | SRX17088844 | SRS14371194 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | WT 3 | strain:AB|age:8 mpf of wide type fish 3|BioSampleModel:Model organism or animal | RNAseq of follicle | s125 | s125 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | WT3.fq.gz | fastq | 3292567800.0 | 21950452.0 | WT3.fq.gz | 0:150 1:0 | A:868410355;C:785426866;G:781134863;T:857556374;N:39342 | 150 | 0 | 868410355 | 785426866 | 781134863 | 857556374 | 39342 | SRX17088844 | SRS14371194 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.94868 | 0.0215 | 0.73673 | 0.49069 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-16 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||
| 70368 | 70368 | SRR21073881 | SRX17088843 | SRS14371193 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | WT 2 | strain:AB|age:8 mpf of wide type fish 2|BioSampleModel:Model organism or animal | RNAseq of follicle | s124 | s124 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | loader:fastq load.py | WT2.fq.gz | fastq | 3252087750.0 | 21680585.0 | WT2.fq.tar.gz | 0:150 | A:844915133;C:783918734;G:794244671;T:828984595;N:24617 | 150 | 844915133 | 783918734 | 794244671 | 828984595 | 24617 | SRX17088843 | SRS14371193 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.93242 | 0.05061 | 0.725 | 0.49837 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-25 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||||||
| 70369 | 70369 | SRR21073882 | SRX17088842 | SRS14371192 | SRP388936 | PRJNA849909 | Danio rerio strain:AB Raw sequence reads | PRJNA849909 | Whole Genome Sequencing | normal ovary of zebrafish | WT 1 | strain:AB|age:8 mpf of wide type fish 1|BioSampleModel:Model organism or animal | RNAseq of follicle | s123 | s123 | normal RNA Seq of ovary | RNA-Seq | TRANSCRIPTOMIC | Oligo-dT | SINGLE | ILLUMINA | Illumina NovaSeq 6000 | SRP388936 | WT1.fq.gz | fastq | 3302333850.0 | 22015559.0 | WT1.fq.gz | 0:0 1:150 | A:865685853;C:788747204;G:788058590;T:859821131;N:21072 | 0 | 150 | 865685853 | 788747204 | 788058590 | 859821131 | 21072 | SRX17088842 | SRS14371192 | SRA1476176 | University of Macau|Faculty of Health Sciences | University of Macau | 1 | 0.94952 | 0.02093 | 0.7376 | 0.49025 | 150 | B | usable mapping rate | illumina | novaseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2022-08-16 | Adult | Adult | Gonad | Reproductive System |
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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");;