{"database": "metadata", "table": "run_metadata", "is_view": false, "human_description_en": "where experiment.library_selection = \"other\", experiment.library_source = \"TRANSCRIPTOMIC\" and tissue_curation_coarse = \"Respiratory System\"", "rows": [[53349, "SRR9849251", "SRX6603836", "SRS5168885", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 6", "kl 14744 d gill", null, "strain:AB|age:3months|sex:female|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 6|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 6", "kl 14744 d gill", "kl 14744 d gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. 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RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  5 mpf  replicate 1", "kl 14562 a gill", null, "strain:AB|age:5months|sex:male|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 1|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  5 mpf  replicate 1", "kl 14562 a gill", "kl 14562 a gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  5 mpf  replicate 5", "kl 14563 c gill", null, "strain:AB|age:5months|sex:female|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 5|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  5 mpf  replicate 5", "kl 14563 c gill", "kl 14563 c gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14563-c-gill_merged_S49-1.fastq.gz kl-14563-c-gill_merged_S49-2.fastq.gz", "fastq fastq", 3023771958.0, 21203385.0, "kl 14563 c gill merged S49 1.fastq.gz", "0:71.29 1:71.32", "A:724268289;C:701710927;G:696152349;T:747721141;N:153919252", 71, 71, null, null, 724268289, 701710927, 696152349, 747721141, 153919252, "SRX6603829", "SRS5168878", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.95184, 0.95462, 0.09513, 0.09444, 0.70386, 0.70506, 0.52039, 0.52251, 76, 76, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53357, "SRR9849259", "SRX6603828", "SRS5168877", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 1", "kl 14744 a gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 1|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 1", "kl 14744 a gill", "kl 14744 a gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14744-a-gill_merged_S3-1.fastq.gz kl-14744-a-gill_merged_S3-2.fastq.gz", "fastq fastq", 4472258246.0, 30417040.0, "kl 14744 a gill merged S3 1.fastq.gz", "0:73.52 1:73.52", "A:1163792021;C:1015967093;G:1005569946;T:1189321143;N:97608043", 73, 73, null, null, 1163792021, 1015967093, 1005569946, 1189321143, 97608043, "SRX6603828", "SRS5168877", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.93243, 0.93488, 0.11957, 0.11821, 0.69043, 0.68982, 0.4947, 0.50103, 76, 76, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53358, "SRR9849260", "SRX6603827", "SRS5168876", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 7", "wt 14560 h gill", null, "strain:AB|age:5months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 7|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 7", "wt 14560 h gill", "wt 14560 h gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-h-gill_merged_S86-1.fastq.gz wt-14560-h-gill_merged_S86-2.fastq.gz", "fastq fastq", 3856374025.0, 26027532.0, "wt 14560 h gill merged S86 1.fastq.gz", "0:74.10 1:74.07", "A:904187535;C:977357747;G:982381061;T:926724178;N:65723504", 74, 74, null, null, 904187535, 977357747, 982381061, 926724178, 65723504, "SRX6603827", "SRS5168876", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.95669, 0.95945, 0.08449, 0.08231, 0.70378, 0.70662, 0.51566, 0.51794, 75, 76, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53359, "SRR9849261", "SRX6603826", "SRS5168875", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 3", "kl 14744 e gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 3|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 3", "kl 14744 e gill", "kl 14744 e gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14744-e-gill_merged_S4-1.fastq.gz kl-14744-e-gill_merged_S4-2.fastq.gz", "fastq fastq", 5367136114.0, 36130715.0, "kl 14744 e gill merged S4 1.fastq.gz", "0:74.28 1:74.27", "A:1423114942;C:1217135684;G:1200462354;T:1454946366;N:71476768", 74, 74, null, null, 1423114942, 1217135684, 1200462354, 1454946366, 71476768, "SRX6603826", "SRS5168875", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.92473, 0.92706, 0.14361, 0.14221, 0.68314, 0.68215, 0.49619, 0.49814, 76, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53360, "SRR9849262", "SRX6603825", "SRS5168874", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 2", "kl 14744 c gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 2|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 2", "kl 14744 c gill", "kl 14744 c gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14744-c-gill_merged_S51-1.fastq.gz kl-14744-c-gill_merged_S51-2.fastq.gz", "fastq fastq", 3781913771.0, 25535680.0, "kl 14744 c gill merged S51 1.fastq.gz", "0:74.05 1:74.06", "A:973851133;C:877578711;G:873528708;T:994449171;N:62506048", 74, 74, null, null, 973851133, 877578711, 873528708, 994449171, 62506048, "SRX6603825", "SRS5168874", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.93396, 0.93615, 0.11943, 0.11847, 0.69428, 0.69597, 0.51454, 0.51378, 76, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53361, "SRR9849263", "SRX6603824", "SRS5168873", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 4", "wt 14560 g gill", null, "strain:AB|age:5months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 4|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 4", "wt 14560 g gill", "wt 14560 g gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-g-gill_merged_S74-1.fastq.gz wt-14560-g-gill_merged_S74-2.fastq.gz", "fastq fastq", 3197383391.0, 23146133.0, "wt 14560 g gill merged S74 1.fastq.gz", "0:68.96 1:69.18", "A:761238423;C:704040317;G:699107362;T:780204404;N:252792885", 68, 69, null, null, 761238423, 704040317, 699107362, 780204404, 252792885, "SRX6603824", "SRS5168873", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.9322, 0.93439, 0.11465, 0.11387, 0.6996, 0.70145, 0.51674, 0.52391, 59, 59, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53362, "SRR9849264", "SRX6603823", "SRS5168872", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 3", "wt 14560 e gill", null, "strain:AB|age:5months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 3|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 3", "wt 14560 e gill", "wt 14560 e gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-e-gill_merged_S37-1.fastq.gz wt-14560-e-gill_merged_S37-2.fastq.gz", "fastq fastq", 6534462524.0, 46930991.0, "wt 14560 e gill merged S37 1.fastq.gz", "0:69.60 1:69.64", "A:1419832692;C:1577789914;G:1592333860;T:1463766163;N:480739895", 69, 69, null, null, 1419832692, 1577789914, 1592333860, 1463766163, 480739895, "SRX6603823", "SRS5168872", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.95759, 0.96007, 0.08549, 0.08527, 0.72352, 0.7263, 0.51737, 0.51106, 76, 71, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53363, "SRR9849265", "SRX6603822", "SRS5168871", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 6", "wt 14560 f gill", null, "strain:AB|age:5months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 6|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 6", "wt 14560 f gill", "wt 14560 f gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-f-gill_merged_S61-1.fastq.gz wt-14560-f-gill_merged_S61-2.fastq.gz", "fastq fastq", 8181016280.0, 56620046.0, "wt 14560 f gill merged S61 1.fastq.gz", "0:72.23 1:72.26", "A:1923562561;C:1974860714;G:1970177126;T:1991223564;N:321192315", 72, 72, null, null, 1923562561, 1974860714, 1970177126, 1991223564, 321192315, "SRX6603822", "SRS5168871", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.95764, 0.95938, 0.08178, 0.08069, 0.69483, 0.6955, 0.4956, 0.49531, 75, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53364, "SRR9849266", "SRX6603821", "SRS5168870", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 5", "wt 14560 b gill", null, "strain:AB|age:5months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 5|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 5", "wt 14560 b gill", "wt 14560 b gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-b-gill_merged_S14-1.fastq.gz wt-14560-b-gill_merged_S14-2.fastq.gz", "fastq fastq", 2362372367.0, 23358970.0, "wt 14560 b gill merged S14 1.fastq.gz", "0:49.78 1:51.36", "A:342145885;C:327654164;G:338531990;T:348076960;N:1005963368", 49, 51, null, null, 342145885, 327654164, 338531990, 348076960, 1005963368, "SRX6603821", "SRS5168870", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.95925, 0.96332, 0.40158, 0.40128, 0.83307, 0.83439, 0.53786, 0.53636, 35, 35, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53365, "SRR9849267", "SRX6603820", "SRS5168869", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 5", "kl 14744 b gill", null, "strain:AB|age:3months|sex:female|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 5|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 5", "kl 14744 b gill", "kl 14744 b gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14744-b-gill_merged_S15-1.fastq.gz kl-14744-b-gill_merged_S15-2.fastq.gz", "fastq fastq", 3896384369.0, 26369685.0, "kl 14744 b gill merged S15 1.fastq.gz", "0:73.87 1:73.89", "A:1006926925;C:896442422;G:893773611;T:1027571320;N:71670091", 73, 73, null, null, 1006926925, 896442422, 893773611, 1027571320, 71670091, "SRX6603820", "SRS5168869", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.93425, 0.93671, 0.10573, 0.10362, 0.68925, 0.69055, 0.50881, 0.50958, 76, 76, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53366, "SRR9849268", "SRX6603819", "SRS5168868", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "\u03b1Klotho  gill  3 mpf  replicate 4", "kl 14744 g gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:aKlotho|Replicate:Bilogical replicate 4|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "Klotho  gill  3 mpf  replicate 4", "kl 14744 g gill", "kl 14744 g gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "kl-14744-g-gill_merged_S40-1.fastq.gz kl-14744-g-gill_merged_S40-2.fastq.gz", "fastq fastq", 4106174367.0, 27588154.0, "kl 14744 g gill merged S40 1.fastq.gz", "0:74.44 1:74.40", "A:1027552543;C:990923882;G:985638754;T:1052538016;N:49521172", 74, 74, null, null, 1027552543, 990923882, 985638754, 1052538016, 49521172, "SRX6603819", "SRS5168868", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.94712, 0.94847, 0.086, 0.08492, 0.69065, 0.69213, 0.50545, 0.50658, 76, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53367, "SRR9849269", "SRX6603818", "SRS5168867", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 2", "wt 14560 c gill", null, "strain:AB|age:5months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 2|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 2", "wt 14560 c gill", "wt 14560 c gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-c-gill_merged_S50-1.fastq.gz wt-14560-c-gill_merged_S50-2.fastq.gz", "fastq fastq", 3502888551.0, 23649590.0, "wt 14560 c gill merged S50 1.fastq.gz", "0:74.05 1:74.07", "A:903995121;C:812069624;G:808206962;T:922560926;N:56055918", 74, 74, null, null, 903995121, 812069624, 808206962, 922560926, 56055918, "SRX6603818", "SRS5168867", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.93602, 0.93796, 0.1196, 0.11851, 0.7054, 0.70642, 0.51487, 0.51576, 76, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53368, "SRR9849270", "SRX6603817", "SRS5168866", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  5 mpf  replicate 1", "wt 14560 a gill", null, "strain:AB|age:5months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 1|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  5 mpf  replicate 1", "wt 14560 a gill", "wt 14560 a gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14560-a-gill_merged_S2-1.fastq.gz wt-14560-a-gill_merged_S2-2.fastq.gz", "fastq fastq", 3961292962.0, 26763233.0, "wt 14560 a gill merged S2 1.fastq.gz", "0:74.00 1:74.01", "A:1030164139;C:909271583;G:896656858;T:1054638293;N:70562089", 74, 74, null, null, 1030164139, 909271583, 896656858, 1054638293, 70562089, "SRX6603817", "SRS5168866", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.93066, 0.93386, 0.11894, 0.11767, 0.70333, 0.70305, 0.52591, 0.5296, 76, 76, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53369, "SRR9849271", "SRX6603816", "SRS5168865", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 8", "wt 14746 i gill", null, "strain:AB|age:3months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 8|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 8", "wt 14746 i gill", "wt 14746 i gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14746-i-gill_merged_S76-1.fastq.gz wt-14746-i-gill_merged_S76-2.fastq.gz", "fastq fastq", 3270182743.0, 22131464.0, "wt 14746 i gill merged S76 1.fastq.gz", "0:73.88 1:73.89", "A:804863458;C:789181461;G:789200500;T:825128130;N:61809194", 73, 73, null, null, 804863458, 789181461, 789200500, 825128130, 61809194, "SRX6603816", "SRS5168865", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.94667, 0.94869, 0.09194, 0.09083, 0.68982, 0.69071, 0.49863, 0.49843, 73, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53370, "SRR9849272", "SRX6603815", "SRS5168864", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 7", "wt 14746 g gill", null, "strain:AB|age:3months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 7|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 7", "wt 14746 g gill", "wt 14746 g gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. ERCC RNA Spike in mix was added for quality control. mRNA was captured using poly T oligos attached beads for library selection.", null, null, "RNA-Seq", "TRANSCRIPTOMIC", "other", "PAIRED", "ILLUMINA", "Illumina HiSeq 2500", null, "SRP216556", null, null, "wt-14746-g-gill_merged_S52-1.fastq.gz wt-14746-g-gill_merged_S52-2.fastq.gz", "fastq fastq", 3993806223.0, 26757111.0, "wt 14746 g gill merged S52 1.fastq.gz", "0:74.64 1:74.63", "A:1042379582;C:926777409;G:917134457;T:1066753507;N:40761268", 74, 74, null, null, 1042379582, 926777409, 917134457, 1066753507, 40761268, "SRX6603815", "SRS5168864", "SRA927891", "Novartis Institutes for Biomedical Research|Chemical Biology and Therapeutics", "Novartis Institutes for Biomedical Research", 2, 0.92989, 0.93168, 0.12566, 0.12387, 0.69483, 0.69398, 0.51742, 0.51246, 75, 75, "B", "B", "biological fallback assumption", "illumina", "hiseq_era", "unknown", "poly_a", "unknown", "bulk", "unknown", "unknown", null, "Germany", "2019-07-27", "Adult", "Adult", "Gill", "Respiratory System"], [53371, "SRR9849273", "SRX6603814", "SRS5168863", "SRP216556", "PRJNA556842", "aKlotho regulates age associated vascular calcification and lifespan in zebrafish", "PRJNA556842", "Transcriptome Analysis", "The hormone aKlotho regulates lifespan in mice as knockouts die early of what appears to be accelerated aging due to hyperphosphatemia and soft tissue calcification. In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 6", "wt 14746 d gill", null, "strain:AB|age:3months|sex:female|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 6|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 6", "wt 14746 d gill", "wt 14746 d gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 4", "wt 14746 h gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 4|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 4", "wt 14746 h gill", "wt 14746 h gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 3", "wt 14746 f gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 3|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 3", "wt 14746 f gill", "wt 14746 f gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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These findings suggest that the gradual loss of aKlotho found in normal aging might give rise to ectopic calcification.", null, null, null, "wildtype  gill  3 mpf  replicate 2", "wt 14746 e gill", null, "strain:AB|age:3months|sex:male|tissue:gills|genotype:wildtype|Replicate:Bilogical replicate 2|BioSampleModel:Model organism or animal", null, null, null, null, null, null, null, null, "wildtype  gill  3 mpf  replicate 2", "wt 14746 e gill", "wt 14746 e gill", "Tissue collection and dissection: Adult zebrafish were euthanized by exposure to chilled water 0 4C. Gills  heart and kidney were collected from 32 individual fish at two time points  namely at 3 mpf and 5 mpf for klotho mutants and wildtype sibling controls AB background; 8 fish per genotype per time point   4 males  4 females for a total of 96 samples. Tissues were dissected in cold PBS and immediately stored in RNALater Stabilization Solution ThermoFisher Cat# AM7021. RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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In contrast  its overexpression increases lifespan. Given the severe mouse phenotype  we generated zebrafish mutants for aklotho as well as its binding partner fibroblast growth factor 23 fgf23. Both mutations cause shortened lifespan in zebrafish  with abrupt onset of behavioral and degenerative physical changes at around five months of age. There is calcification of vessels throughout the body  most dramatically in the outflow tract of the heart  the bulbus arteriosus BA. This calcification is associated with ectopic activation of osteoclast differentiation pathways. 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RNALater was removed post an overnight incubation at 4C  and samples were stored at  80C until processing. RNA extraction: All tissues were homogenized using the TissueLyser II Qiagen plus Lysis buffer containing  mercaptoethanol and stored at  80C. RNA extraction was performed using the automated protocol in the QIAcube workstation utilizing the RNeasy Fibrous Tissue Mini kit Qiagen Cat No./ID: 74704. RNA integrity and quality were assessed by Agilent TapeStation using High Sensitivity RNA ScreenTapes. Samples were normalized and 300ng of RNA was used for library prep for each sample. 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