run_metadata
23 rows where experiment.library_selection = "size fractionation", experiment.library_strategy = "RNA-Seq" 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 36273 | 36273 | SRR298566 | SRX079844 | SRS212650 | SRP007331 | PRJNA141525 | Tdrd1 acts as a molecular scaffold for Piwi proteins and piRNA targets in zebrafish. | GSE29418 | Transcriptome Analysis | RNA libraries from immunoprecipitates of Tdrd1 Ziwi and Zili total testis RNA total RNA from 3 wpf wild type and tdrd1 mutant gonads. Overall design: Both size selected and non size selected libraries were made. Sequencing was performed using Illumina platform. | pubmed:21743441 | WTTESTIS | GSM727523 | tissue:adult testis extract|strain:TL | WTTESTIS | three prime adapter sequences were trimmed and inserts longer than 18 nt were mapped to the D. rerio genome Zv9. | adult testis extract | Tissue was homogenized in trizol and total RNA was isolated. RNAs ranging from 18 35 nucleotides were size selected from gel. For cDNA synthesis the RNA molecules in the immunoprecipitated fraction were first poly A tailed using polyApolymerase followed by ligation of synthetic RNA adapter to the five prime phosphate. First strand cDNA synthesis was then performed using an oligodT linker primer and M MLVRNase H reverse transcriptase. cDNA was PCR amplified with adapter specific primers and used in Illumina sequencing. | strain:TL | GSM727523 | GSM727523: WTTESTIS | GSM727523: WTTESTIS | GSM727523: WTTESTIS | 1 | GEO Accession:GSM727523 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP007331 | read name barcode proc directive:ignore | WTTESTIS.fastq | fastq | 732997980.0 | 20361055.0 | GSM727523 1 | 0:36 | 36 | SRX079844 | SRS212650 | SRA039167 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.08155 | 0.07176 | 0.97851 | 0.52359 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2011-05-20 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||||
| 36274 | 36274 | SRR298565 | SRX079843 | SRS212649 | SRP007331 | PRJNA141525 | Tdrd1 acts as a molecular scaffold for Piwi proteins and piRNA targets in zebrafish. | GSE29418 | Transcriptome Analysis | RNA libraries from immunoprecipitates of Tdrd1 Ziwi and Zili total testis RNA total RNA from 3 wpf wild type and tdrd1 mutant gonads. Overall design: Both size selected and non size selected libraries were made. Sequencing was performed using Illumina platform. | pubmed:21743441 | WT3WK | GSM727522 | tissue:3 wpf whole gonads|strain:TL | WT3WK | three prime adapter sequences were trimmed and inserts longer than 18 nt were mapped to the D. rerio genome Zv9. | 3 wpf whole gonads | Tissue was homogenized in trizol and total RNA was isolated. RNAs ranging from 18 35 nucleotides were size selected from gel. For cDNA synthesis the RNA molecules in the immunoprecipitated fraction were first poly A tailed using polyApolymerase followed by ligation of synthetic RNA adapter to the five prime phosphate. First strand cDNA synthesis was then performed using an oligodT linker primer and M MLVRNase H reverse transcriptase. cDNA was PCR amplified with adapter specific primers and used in Illumina sequencing. | strain:TL | GSM727522 | GSM727522: WT3WK | GSM727522: WT3WK | GSM727522: WT3WK | 1 | GEO Accession:GSM727522 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP007331 | read name barcode proc directive:ignore | WT3WK.fastq | fastq | 365473116.0 | 10152031.0 | GSM727522 1 | 0:36 | 36 | SRX079843 | SRS212649 | SRA039167 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.09055 | 0.0603 | 0.97798 | 0.44571 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2011-05-20 | Larval | Larval | Gonad | Reproductive System | |||||||||||||||||||||||
| 36275 | 36275 | SRR298564 | SRX079842 | SRS212648 | SRP007331 | PRJNA141525 | Tdrd1 acts as a molecular scaffold for Piwi proteins and piRNA targets in zebrafish. | GSE29418 | Transcriptome Analysis | RNA libraries from immunoprecipitates of Tdrd1 Ziwi and Zili total testis RNA total RNA from 3 wpf wild type and tdrd1 mutant gonads. Overall design: Both size selected and non size selected libraries were made. Sequencing was performed using Illumina platform. | pubmed:21743441 | TDRD1WK3 | GSM727521 | tissue:3 wpf tdrd1 mutant gonads|strain:TL | TDRD1WK3 | three prime adapter sequences were trimmed and inserts longer than 18 nt were mapped to the D. rerio genome Zv9. | 3 wpf tdrd1 mutant gonads | Tissue was homogenized in trizol and total RNA was isolated. RNAs ranging from 18 35 nucleotides were size selected from gel. For cDNA synthesis the RNA molecules in the immunoprecipitated fraction were first poly A tailed using polyApolymerase followed by ligation of synthetic RNA adapter to the five prime phosphate. First strand cDNA synthesis was then performed using an oligodT linker primer and M MLVRNase H reverse transcriptase. cDNA was PCR amplified with adapter specific primers and used in Illumina sequencing. | strain:TL | GSM727521 | GSM727521: TDRD1WK3 | GSM727521: TDRD1WK3 | GSM727521: TDRD1WK3 | 1 | GEO Accession:GSM727521 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer II | <SPOT_DESCRIPTOR><SPOT_DECODE_SPEC><SPOT_LENGTH>36</SPOT_LENGTH><READ_SPEC><READ_INDEX>0</READ_INDEX><READ_CLASS>Application Read</READ_CLASS><READ_TYPE>Forward</READ_TYPE><BASE_COORD>1</BASE_COORD></READ_SPEC></SPOT_DECODE_SPEC></SPOT_DESCRIPTOR> | SRP007331 | read name barcode proc directive:ignore | TDRD1WK3.fastq | fastq | 369931536.0 | 10275876.0 | GSM727521 1 | 0:36 | 36 | SRX079842 | SRS212648 | SRA039167 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.08303 | 0.04674 | 0.97938 | 0.35673 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2011-05-20 | Larval | Larval | Gonad | Reproductive System | |||||||||||||||||||||||
| 36514 | 36514 | SRR578923 | SRX190981 | SRS366702 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJD male | GSM1014087 | source name:Testes|sex:male|strain:SJD|development stage:Adult|tissue:Testes | SJD male | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Testes | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:male|strain:SJD|developmental stage:Adult|tissue:Testes | GSM1014087 | GSM1014087: SJD male; Danio rerio; RNA Seq | GSM1014087 1 | 1 | GEO Accession:GSM1014087 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | SJD_Male.fastq | fastq | 869956128.0 | 24165448.0 | GSM1014087 r1 | 0:36 | A:216078167;C:187750746;G:231408128;T:234642875;N:76212 | 36 | 216078167 | 187750746 | 231408128 | 234642875 | 76212 | SRX190981 | SRS366702 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.27444 | 0.19385 | 0.92478 | 0.49214 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36515 | 36515 | SRR578922 | SRX190980 | SRS366701 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | Tu Male | GSM1014086 | source name:Testes|sex:male|strain:Tu|development stage:Adult|tissue:Testes | Tu Male | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Testes | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:male|strain:Tu|developmental stage:Adult|tissue:Testes | GSM1014086 | GSM1014086: Tu Male; Danio rerio; RNA Seq | GSM1014086 1 | 1 | GEO Accession:GSM1014086 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 908421696.0 | 25233936.0 | GSM1014086 r1 | 0:36 | A:222765185;C:198165182;G:240641436;T:246807325;N:42568 | 36 | 222765185 | 198165182 | 240641436 | 246807325 | 42568 | SRX190980 | SRS366701 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.1451 | 0.10199 | 0.95128 | 0.45517 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36516 | 36516 | SRR578921 | SRX190979 | SRS366700 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF2 Individual 2 | GSM1014085 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF2 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014085 | GSM1014085: TuxSJDF2 Individual 2; Danio rerio; RNA Seq | GSM1014085 1 | 1 | GEO Accession:GSM1014085 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 383509188.0 | 10653033.0 | GSM1014085 r1 | 0:36 | A:105355133;C:85084746;G:89408418;T:103592177;N:68714 | 36 | 105355133 | 85084746 | 89408418 | 103592177 | 68714 | SRX190979 | SRS366700 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.14582 | 0.10997 | 0.96175 | 0.35151 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36517 | 36517 | SRR578920 | SRX190978 | SRS366699 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF2 Individual 1 | GSM1014084 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF2 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014084 | GSM1014084: TuxSJDF2 Individual 1; Danio rerio; RNA Seq | GSM1014084 1 | 1 | GEO Accession:GSM1014084 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | TuxSJDF1_Individual_1.fastq | fastq | 464899752.0 | 12913882.0 | GSM1014084 r1 | 0:36 | A:140830427;C:93401413;G:113254459;T:117332119;N:81334 | 36 | 140830427 | 93401413 | 113254459 | 117332119 | 81334 | SRX190978 | SRS366699 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.43194 | 0.32 | 0.93154 | 0.3438 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36518 | 36518 | SRR578919 | SRX190977 | SRS366698 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF2 | GSM1014083 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014083 | GSM1014083: TuxSJDF2; Danio rerio; RNA Seq | GSM1014083 1 | 1 | GEO Accession:GSM1014083 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | TuxSJDF2.fastq | fastq | 1036162620.0 | 28782295.0 | GSM1014083 r1 | 0:36 | A:268457303;C:215700792;G:273583173;T:278046713;N:374639 | 36 | 268457303 | 215700792 | 273583173 | 278046713 | 374639 | SRX190977 | SRS366698 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.16399 | 0.12914 | 0.9517 | 0.52232 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36519 | 36519 | SRR578918 | SRX190976 | SRS366697 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF1 Individual 2 | GSM1014082 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF1 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014082 | GSM1014082: TuxSJDF1 Individual 2; Danio rerio; RNA Seq | GSM1014082 1 | 1 | GEO Accession:GSM1014082 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 344764980.0 | 9576805.0 | GSM1014082 r1 | 0:36 | A:90252809;C:80943703;G:83338280;T:90171695;N:58493 | 36 | 90252809 | 80943703 | 83338280 | 90171695 | 58493 | SRX190976 | SRS366697 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.18861 | 0.14536 | 0.95335 | 0.54431 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36520 | 36520 | SRR578917 | SRX190975 | SRS366696 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF1 Individual 1 | GSM1014081 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF1 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014081 | GSM1014081: TuxSJDF1 Individual 1; Danio rerio; RNA Seq | GSM1014081 1 | 1 | GEO Accession:GSM1014081 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | TuxSJDF2_Individual_1.fastq | fastq | 373504320.0 | 10375120.0 | GSM1014081 r1 | 0:36 | A:96550943;C:89937876;G:87356943;T:99426239;N:232319 | 36 | 96550943 | 89937876 | 87356943 | 99426239 | 232319 | SRX190975 | SRS366696 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.15362 | 0.12272 | 0.95943 | 0.56453 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36521 | 36521 | SRR578916 | SRX190974 | SRS366695 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | TuxSJDF1 | GSM1014080 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | TuxSJDF1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014080 | GSM1014080: TuxSJDF1; Danio rerio; RNA Seq | GSM1014080 1 | 1 | GEO Accession:GSM1014080 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | TuxSJDF1.fastq | fastq | 1031108904.0 | 28641914.0 | GSM1014080 r1 | 0:36 | A:270773113;C:213123466;G:267237418;T:279702377;N:272530 | 36 | 270773113 | 213123466 | 267237418 | 279702377 | 272530 | SRX190974 | SRS366695 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.15469 | 0.12537 | 0.95457 | 0.48819 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36522 | 36522 | SRR578915 | SRX190973 | SRS366694 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | Tu P0 Individual 2 | GSM1014079 | source name:Ovary|sex:female|strain:Tu|development stage:Adult|tissue:Ovary | Tu P0 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Tu|developmental stage:Adult|tissue:Ovary | GSM1014079 | GSM1014079: Tu P0 Individual 2; Danio rerio; RNA Seq | GSM1014079 1 | 1 | GEO Accession:GSM1014079 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 464586408.0 | 12905178.0 | GSM1014079 r1 | 0:36 | A:150621423;C:99131637;G:92380585;T:122374816;N:77947 | 36 | 150621423 | 99131637 | 92380585 | 122374816 | 77947 | SRX190973 | SRS366694 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.0937 | 0.05289 | 0.96546 | 0.60026 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36523 | 36523 | SRR578914 | SRX190972 | SRS366693 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | Tu P0 Individual 1 | GSM1014078 | source name:Ovary|sex:female|strain:Tu|development stage:Adult|tissue:Ovary | Tu P0 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Tu|developmental stage:Adult|tissue:Ovary | GSM1014078 | GSM1014078: Tu P0 Individual 1; Danio rerio; RNA Seq | GSM1014078 1 | 1 | GEO Accession:GSM1014078 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 427172796.0 | 11865911.0 | GSM1014078 r1 | 0:36 | A:135500495;C:91385480;G:87823245;T:112202150;N:261426 | 36 | 135500495 | 91385480 | 87823245 | 112202150 | 261426 | SRX190972 | SRS366693 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.1368 | 0.09652 | 0.95142 | 0.49555 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36524 | 36524 | SRR578913 | SRX190971 | SRS366692 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | Tu P0 | GSM1014077 | source name:Ovary|sex:female|strain:Tu|development stage:Adult|tissue:Ovary | Tu P0 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Tu|developmental stage:Adult|tissue:Ovary | GSM1014077 | GSM1014077: Tu P0; Danio rerio; RNA Seq | GSM1014077 1 | 1 | GEO Accession:GSM1014077 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 967772772.0 | 26882577.0 | GSM1014077 r1 | 0:36 | A:227085973;C:218180545;G:249458631;T:273002038;N:45585 | 36 | 227085973 | 218180545 | 249458631 | 273002038 | 45585 | SRX190971 | SRS366692 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.14418 | 0.1135 | 0.95818 | 0.51074 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36525 | 36525 | SRR578912 | SRX190970 | SRS366691 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF2 Individual 2 | GSM1014076 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF2 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014076 | GSM1014076: SJDxTuF2 Individual 2; Danio rerio; RNA Seq | GSM1014076 1 | 1 | GEO Accession:GSM1014076 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 347475024.0 | 9652084.0 | GSM1014076 r1 | 0:36 | A:91189258;C:81789488;G:84551251;T:89882775;N:62252 | 36 | 91189258 | 81789488 | 84551251 | 89882775 | 62252 | SRX190970 | SRS366691 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.15872 | 0.12439 | 0.95848 | 0.56717 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36526 | 36526 | SRR578911 | SRX190969 | SRS366690 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF2 Individual 1 | GSM1014075 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF2 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014075 | GSM1014075: SJDxTuF2 Individual 1; Danio rerio; RNA Seq | GSM1014075 1 | 1 | GEO Accession:GSM1014075 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 400137228.0 | 11114923.0 | GSM1014075 r1 | 0:36 | A:107143937;C:91495000;G:94706504;T:106722021;N:69766 | 36 | 107143937 | 91495000 | 94706504 | 106722021 | 69766 | SRX190969 | SRS366690 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.15753 | 0.12463 | 0.95538 | 0.5649 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36527 | 36527 | SRR578910 | SRX190968 | SRS366689 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF2 | GSM1014074 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014074 | GSM1014074: SJDxTuF2; Danio rerio; RNA Seq | GSM1014074 1 | 1 | GEO Accession:GSM1014074 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | SJDxTuF2.fastq | fastq | 958492116.0 | 26624781.0 | GSM1014074 r1 | 0:36 | A:261275440;C:193944805;G:248348765;T:254793050;N:130056 | 36 | 261275440 | 193944805 | 248348765 | 254793050 | 130056 | SRX190968 | SRS366689 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.20051 | 0.16387 | 0.94653 | 0.53263 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36528 | 36528 | SRR578909 | SRX190967 | SRS366688 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF1 Individual 2 | GSM1014073 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF1 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014073 | GSM1014073: SJDxTuF1 Individual 2; Danio rerio; RNA Seq | GSM1014073 1 | 1 | GEO Accession:GSM1014073 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 435761532.0 | 12104487.0 | GSM1014073 r1 | 0:36 | A:120580697;C:105605593;G:91379055;T:117787426;N:408761 | 36 | 120580697 | 105605593 | 91379055 | 117787426 | 408761 | SRX190967 | SRS366688 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.07215 | 0.05695 | 0.97557 | 0.48838 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36529 | 36529 | SRR578908 | SRX190966 | SRS366687 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF1 Individual 1 | GSM1014072 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF1 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014072 | GSM1014072: SJDxTuF1 Individual 1; Danio rerio; RNA Seq | GSM1014072 1 | 1 | GEO Accession:GSM1014072 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 378296532.0 | 10508237.0 | GSM1014072 r1 | 0:36 | A:109216358;C:76585213;G:90165899;T:102085771;N:243291 | 36 | 109216358 | 76585213 | 90165899 | 102085771 | 243291 | SRX190966 | SRS366687 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.13684 | 0.10794 | 0.96335 | 0.49651 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36530 | 36530 | SRR578907 | SRX190965 | SRS366686 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJDxTuF1 | GSM1014071 | source name:Ovary|sex:female|strain:Hybrid SJD and Tu|development stage:Adult|tissue:Ovary | SJDxTuF1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:Hybrid SJD and Tu|developmental stage:Adult|tissue:Ovary | GSM1014071 | GSM1014071: SJDxTuF1; Danio rerio; RNA Seq | GSM1014071 1 | 1 | GEO Accession:GSM1014071 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | 1047688380.0 | 29102455.0 | GSM1014071 r1 | 0:36 | A:277032474;C:213232299;G:269309034;T:288068877;N:45696 | 36 | 277032474 | 213232299 | 269309034 | 288068877 | 45696 | SRX190965 | SRS366686 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.1858 | 0.15153 | 0.95006 | 0.51345 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||||
| 36531 | 36531 | SRR578906 | SRX190964 | SRS366685 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJD P0 Individual 2 | GSM1014070 | source name:Ovary|sex:female|strain:SJD|development stage:Adult|tissue:Ovary | SJD P0 Individual 2 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:SJD|developmental stage:Adult|tissue:Ovary | GSM1014070 | GSM1014070: SJD P0 Individual 2; Danio rerio; RNA Seq | GSM1014070 1 | 1 | GEO Accession:GSM1014070 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | SJD_P0_Individual_2.fastq | fastq | 392951772.0 | 10915327.0 | GSM1014070 r1 | 0:36 | A:126709476;C:82393458;G:82997127;T:100597122;N:254589 | 36 | 126709476 | 82393458 | 82997127 | 100597122 | 254589 | SRX190964 | SRS366685 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.12786 | 0.10199 | 0.95724 | 0.52026 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36532 | 36532 | SRR578905 | SRX190963 | SRS366684 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJD P0 Individual 1 | GSM1014069 | source name:Ovary|sex:female|strain:SJD|development stage:Adult|tissue:Ovary | SJD P0 Individual 1 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:SJD|developmental stage:Adult|tissue:Ovary | GSM1014069 | GSM1014069: SJD P0 Individual 1; Danio rerio; RNA Seq | GSM1014069 1 | 1 | GEO Accession:GSM1014069 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | SJD_P0_Individual_1.fastq | fastq | 379882512.0 | 10552292.0 | GSM1014069 r1 | 0:36 | A:122444116;C:80302064;G:76948943;T:99839311;N:348078 | 36 | 122444116 | 80302064 | 76948943 | 99839311 | 348078 | SRX190963 | SRS366684 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.21364 | 0.16206 | 0.94268 | 0.45306 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | Adult | Adult | Gonad | Reproductive System | |||||||||||||||||||
| 36533 | 36533 | SRR578904 | SRX190962 | SRS366683 | SRP015982 | PRJNA176481 | Small RNA analysis of Tu And SJD zebrafish strain and their progeny | GSE41299 | Transcriptome Analysis | Small RNA libraries from total RNA isolated from adult ovaries Overall design: Small RNA libraries were derived from Ovaries of the Founder strain and their offspring and their reciprocal offspring. RNA from 5 individual ovaries was pooled . | pubmed:23335638 | SJD P0 | GSM1014068 | source name:Ovary|sex:female|strain:SJD|development stage:Adult|tissue:Ovary | SJD P0 | Barcode splitting and adapter trimming performed using custom scripts. Barcode is the first 4 bases of the reads except for libraries Tu Male Tu P0 SJD Male SJD P0 SJDxTuF1 TuxSJDF1 TuxSJDF2 and SJDxTuF2 which do not have a barcode. three prime adapter seqeunce starts with 'TCGTATG'. Reads were mapped to D.rerio genome assembly using megablast software. Genome build: Zv9 Supplementary files format and content: Text file with read counts | Ovary | Total RNA was isolated using fast protK mediated lysis and Trizol LS protocols. five prime and three prime adaptors were ligated. RNA was not treated with any enzymes before ligation steps. | Animals were grown under standard conditioni | gender:female|strain:SJD|developmental stage:Adult|tissue:Ovary | GSM1014068 | GSM1014068: SJD P0; Danio rerio; RNA Seq | GSM1014068 1 | 1 | GEO Accession:GSM1014068 | RNA-Seq | TRANSCRIPTOMIC | size fractionation | SINGLE | ILLUMINA | Illumina Genome Analyzer IIx | SRP015982 | SJD_P0.fastq | fastq | 837950832.0 | 23276412.0 | GSM1014068 r1 | 0:36 | A:217386642;C:179519865;G:217337232;T:223633685;N:73408 | 36 | 217386642 | 179519865 | 217337232 | 223633685 | 73408 | SRX190962 | SRS366683 | SRA059229 | GEO | European Research Institute for the Biology of Ageing, University Medical Center Groningen | 1 | 0.26607 | 0.21631 | 0.93789 | 0.46928 | 36 | B | usable mapping rate | illumina | early_illumina | unknown | size_fractionation | unknown | bulk | unknown | unknown | Netherlands | 2012-10-03 | 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");;