{"database": "metadata", "table": "run_metadata", "is_view": false, "human_description_en": "where experiment.library_layout = \"PAIRED\", experiment.library_selection = \"RANDOM PCR\" and tissue_curation = \"Embryo Imprecise\"", "rows": [[55655, "SRR10674410", "SRX7351703", "SRS5811186", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. 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To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "Cntrol1", null, "isolate:biologocal replicate 16|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050116", "bps050116", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "Cntrol1_1.fq.gz Cntrol1_2.fq.gz", "fastq fastq", 6766663000.0, 67666630.0, "Cntrol1 1.fq.gz", "0:100 1:100", "A:1825736389;C:1564390057;G:1532835305;T:1842876742;N:824507", 100, 100, null, null, 1825736389, 1564390057, 1532835305, 1842876742, 824507, "SRX7351693", "SRS5811174", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94047, null, 0.12338, null, 0.68893, null, 0.46407, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55666, "SRR10674421", "SRX7351692", "SRS5811176", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 1000 3", null, "isolate:biologocal replicate 15|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050115", "bps050115", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_1000_3_1.fq.gz BPS_1000_3_2.fq.gz", "fastq fastq", 6507622200.0, 65076222.0, "BPS 1000 3 1.fq.gz", "0:100 1:100", "A:1735402948;C:1525938362;G:1493787016;T:1751945676;N:548198", 100, 100, null, null, 1735402948, 1525938362, 1493787016, 1751945676, 548198, "SRX7351692", "SRS5811176", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94304, null, 0.10593, null, 0.6842, null, 0.46348, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55667, "SRR10674422", "SRX7351691", "SRS5811173", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 1000 2", null, "isolate:biologocal replicate 14|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050114", "bps050114", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_1000_2_1.fq.gz BPS_1000_2_2.fq.gz", "fastq fastq", 6740712000.0, 67407120.0, "BPS 1000 2 1.fq.gz", "0:100 1:100", "A:1816870993;C:1562402111;G:1527381283;T:1833284067;N:773546", 100, 100, null, null, 1816870993, 1562402111, 1527381283, 1833284067, 773546, "SRX7351691", "SRS5811173", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94327, null, 0.11511, null, 0.70033, null, 0.4551, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55668, "SRR10674423", "SRX7351690", "SRS5811175", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 1000 1", null, "isolate:biologocal replicate 13|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050113", "bps050113", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_1000_1_1.fq.gz BPS_1000_1_2.fq.gz", "fastq fastq", 6727750400.0, 67277504.0, "BPS 1000 1 1.fq.gz", "0:100 1:100", "A:1803578734;C:1568712705;G:1535618959;T:1819016739;N:823263", 100, 100, null, null, 1803578734, 1568712705, 1535618959, 1819016739, 823263, "SRX7351690", "SRS5811175", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94457, null, 0.1118, null, 0.69087, null, 0.46815, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55669, "SRR10674424", "SRX7351689", "SRS5811172", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 100 3", null, "isolate:biologocal replicate 12|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050112", "bps050112", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_100_3_1.fq.gz BPS_100_3_2.fq.gz", "fastq fastq", 6962431800.0, 69624318.0, "BPS 100 3 1.fq.gz", "0:100 1:100", "A:1865300693;C:1624120289;G:1585691091;T:1886538935;N:780792", 100, 100, null, null, 1865300693, 1624120289, 1585691091, 1886538935, 780792, "SRX7351689", "SRS5811172", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94581, null, 0.10195, null, 0.68288, null, 0.47174, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55670, "SRR10674425", "SRX7351688", "SRS5811171", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 100 2", null, "isolate:biologocal replicate 11|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050111", "bps050111", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_100_2_1.fq.gz BPS_100_2_2.fq.gz", "fastq fastq", 7201035800.0, 72010358.0, "BPS 100 2 1.fq.gz", "0:100 1:100", "A:2115590854;C:1489181336;G:1459936470;T:2135514629;N:812511", 100, 100, null, null, 2115590854, 1489181336, 1459936470, 2135514629, 812511, "SRX7351688", "SRS5811171", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.90678, null, 0.29289, null, 0.70735, null, 0.49554, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55671, "SRR10674426", "SRX7351687", "SRS5811170", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 0 1 2", null, "isolate:biologocal replicate 2|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050102", "bps050102", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_0_1_2_1.fq.gz BPS_0_1_2_2.fq.gz", "fastq fastq", 7022382800.0, 70223828.0, "BPS 0 1 2 1.fq.gz", "0:100 1:100", "A:1853514579;C:1663935080;G:1635277415;T:1869136960;N:518766", 100, 100, null, null, 1853514579, 1663935080, 1635277415, 1869136960, 518766, "SRX7351687", "SRS5811170", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94712, null, 0.09313, null, 0.6814, null, 0.47256, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [55672, "SRR10674427", "SRX7351686", "SRS5811167", "SRP237283", "PRJNA595113", "Transcriptomic responses of Bisphenol S on zebrafish", "PRJNA595113", "Other", "To better understand the multiple interacting molecular mechanisms that are altered during BPS exposure  global transcriptome sequencing RNA Seq was performed in embryonic fish to quantify expression levels of transcripts with a high sensitivity and broad genome coverage post BPS treatment19. To better understand sensitivities of fish to BPS toxicity and the mechanisms that regulate expression of transcripts altered by BPS exposure  we evaluated morphological and transcriptional effects in using environmentally relevant concentrations.", null, null, null, null, "BPS 0 1 1", null, "isolate:biologocal replicate 1|age:120hpf|sex:not collected|tissue:embryo|collection date:2018 05 01|geo loc name:China:Guangdong|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Transcriptomic responses of Bisphenol S", "bps050101", "bps050101", "An Agilent 2100 bioanalyzer chip was used to determine RNA integrity score Agilent  Santa Clara  CA  USA with only high quality RNA samples 28 S:18 S=2.02.2  RIN>9.0 used to construct libraries following a standardized procedure at the Beijing Genome Institute BGI; Shenzhen  China . The libraries were sequenced at the Beijing Genomics Institute BGI  Shenzhen  China on a BGISEQ500 platform with 50 bp single end reads  under three replicates per treatment group.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "BGISEQ", "BGISEQ-500", null, "SRP237283", null, null, "BPS_0_1_1_1.fq.gz BPS_0_1_1_2.fq.gz", "fastq fastq", 7013900400.0, 70139004.0, "BPS 0 1 1 1.fq.gz", "0:100 1:100", "A:1885826391;C:1629114228;G:1597181244;T:1901261511;N:517026", 100, 100, null, null, 1885826391, 1629114228, 1597181244, 1901261511, 517026, "SRX7351686", "SRS5811167", "SRA1010884", "Southern University of Science and Technology|School of Environmental Science and Engineering", "Southern University of Science and Technology", 1, 0.94226, null, 0.11616, null, 0.69014, null, 0.45679, null, 100, null, "B", null, "usable mapping rate", "bgi", "bgi", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2019-12-12", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [64197, "SRR14319883", "SRX10675035", "SRS8769036", "SRP316198", "PRJNA724884", "Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and terfa compromised zebrafish embryos", "PRJNA724884", "Other", "The goals of this study are to compare NGS in 3dpf zebrafish embryo post knockout terfa telomere repeats binding factor 2. In order to investigate the role of terfa in DDR  telomere protection and neuro development.", null, null, null, null, "yyl homo zf rep2", null, "replicate:2|date:2/20/2021/3pm|breed:AB|age:10 day|dev stage:embryo|sex:not determined|tissue:embryo|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "RNA Seq of danio rerio: 3d embryos", "LDA9530", "LDA9530", "RNA libraries were prepared for sequencing using standard Illumina protocols", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP316198", null, null, "TRF2_homozygous_3d_2_LDA9530Aligned.sortedByCoord.out.bam", "bam", 13532124350.0, 45108312.0, "TRF2 homozygous 3d 2 LDA9530Aligned.sortedByCoord.out.bam", "0:150.00 1:150.00", "A:3411777260;C:3360449196;G:3332955645;T:3425874531;N:1067718", 150, 150, null, null, 3411777260, 3360449196, 3332955645, 3425874531, 1067718, "SRX10675035", "SRS8769036", "SRA1223267", "Ruijin hospital, Shanghai, China|Emergency Medchine", "Ruijin hospital, Shanghai, China", 2, 0.96358, 0.96219, 0.06413, 0.06452, 0.67101, 0.67304, 0.45519, 0.45225, 150, 150, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2021-04-24", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [64198, "SRR14319884", "SRX10675034", "SRS8769035", "SRP316198", "PRJNA724884", "Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and terfa compromised zebrafish embryos", "PRJNA724884", "Other", "The goals of this study are to compare NGS in 3dpf zebrafish embryo post knockout terfa telomere repeats binding factor 2. In order to investigate the role of terfa in DDR  telomere protection and neuro development.", null, null, null, null, "yyl homo zf rep1", null, "replicate:1|date:2/20/2021/2pm|breed:AB|age:9 day|dev stage:embryo|sex:not determined|tissue:embryo|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "RNA Seq of danio rerio: 3d embryos", "LDA9528", "LDA9528", "RNA libraries were prepared for sequencing using standard Illumina protocols", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP316198", null, "assembly:GRCz11", "TRF2_homozygous_3d_1_LDA9528Aligned.sortedByCoord.out.bam", "bam", 14927377118.0, 51943892.0, "TRF2 homozygous 3d 1 LDA9528Aligned.sortedByCoord.out.bam", "0:143.69 1:143.69", "A:3703977593;C:3766420543;G:3739925195;T:3715825628;N:1228159", 143, 143, null, null, 3703977593, 3766420543, 3739925195, 3715825628, 1228159, "SRX10675034", "SRS8769035", "SRA1223267", "Ruijin hospital, Shanghai, China|Emergency Medchine", "Ruijin hospital, Shanghai, China", 2, 0.96471, 0.96437, 0.0498, 0.05004, 0.66906, 0.67036, 0.45421, 0.45111, 98, 98, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2021-05-17", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [64199, "SRR14319885", "SRX10675033", "SRS8769034", "SRP316198", "PRJNA724884", "Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and terfa compromised zebrafish embryos", "PRJNA724884", "Other", "The goals of this study are to compare NGS in 3dpf zebrafish embryo post knockout terfa telomere repeats binding factor 2. 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In order to investigate the role of terfa in DDR  telomere protection and neuro development.", null, null, null, null, "yyl hybrid zf rep2", null, "replicate:2|date:2/15/2021/11am|breed:AB|age:7 day|dev stage:embryo|sex:not determined|tissue:embryo|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "RNA Seq of danio rerio: 3d embryos", "LDA9526", "LDA9526", "RNA libraries were prepared for sequencing using standard Illumina protocols", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "RANDOM PCR", "PAIRED", "ILLUMINA", "HiSeq X Ten", null, "SRP316198", null, null, "TRF2_hybrid_3d_2_LDA9526Aligned.sortedByCoord.out.bam", "bam", 13705312262.0, 45685613.0, "TRF2 hybrid 3d 2 LDA9526Aligned.sortedByCoord.out.bam", "0:150.00 1:150.00", "A:3456147807;C:3403904273;G:3377881707;T:3466298988;N:1079487", 150, 150, null, null, 3456147807, 3403904273, 3377881707, 3466298988, 1079487, "SRX10675032", "SRS8769033", "SRA1223267", "Ruijin hospital, Shanghai, China|Emergency Medchine", "Ruijin hospital, Shanghai, China", 2, 0.96349, 0.96378, 0.06028, 0.06096, 0.66296, 0.66655, 0.46411, 0.4594, 150, 150, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "random_priming", "unknown", "bulk", "unknown", "unknown", null, "China", "2021-04-24", "Larval", "Larval", "Embryo Imprecise", "All anatomical structures"], [64201, "SRR14319887", "SRX10675031", "SRS8769032", "SRP316198", "PRJNA724884", "Next Generation Sequencing Facilitates Quantitative Analysis of Wild Type and terfa compromised zebrafish embryos", "PRJNA724884", "Other", "The goals of this study are to compare NGS in 3dpf zebrafish embryo post knockout terfa telomere repeats binding factor 2. 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