run_metadata
12 rows where technology = "smartseq", tissue_curation = "Ear" and tissue_curation_coarse = "Sensory System"
This data as json, CSV (advanced)
| Link | rowid ▼ | run.accession | experiment.accession | sample.accession | study.accession | bioproject | study.title | study.alias | study.type | study.abstract | study.attributes | study.PMIDs | sample.description | sample.title | sample.alias | sample.centername | sample.attributes | GEOsample.title | GEOsample.dataprocessing | GEOsample.source | GEOsample.treatmentprotocol | GEOsample.extractprotocol | GEOsample.growthprotocol | GEOsample.characteristics | GEOsample.accession | experiment.title | experiment.alias | experiment.library_name | experiment.design_description | experiment.library_construction_protocol | experiment.attributes | experiment.library_strategy | experiment.library_source | experiment.library_selection | experiment.library_layout | experiment.platform | experiment.instrument_model | experiment.spot_descriptor | experiment.study_ref | run.title | run.attributes | run.filename | run.semantic_name | run.total_bases | run.total_spots | run.alias | run.read_lengths | run.base_counts | run.r1_length | run.r2_length | run.r3_length | run.r4_length | run.Acount | run.Ccount | run.Gcount | run.Tcount | run.Ncount | run.experiment | run.pool_member | submission.accession | submission.srasource | submission.bioprojectsource | seqdetective.n_mates | seqdetective.mapping_rate.mate1 | seqdetective.mapping_rate.mate2 | seqdetective.nofeature_rate.mate1 | seqdetective.nofeature_rate.mate2 | seqdetective.sparsity.mate1 | seqdetective.sparsity.mate2 | seqdetective.pos_strand_rate.mate1 | seqdetective.pos_strand_rate.mate2 | seqdetective.readlen.mate1 | seqdetective.readlen.mate2 | seqdetective.judgement.mate1 | seqdetective.judgement.mate2 | seqdetective.judgement.reason | platform_family | instrument_generation | read_bias | selection_class | prep_kit | sc_or_bulk | tech_class | technology | tech_variant | submission.bioprojectsource.country | earliest_date | devstage_curation | devstage_curation_coarse | tissue_curation | tissue_curation_coarse |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 41685 | 41685 | SRR5120134 | SRX2435377 | SRS1870364 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP neg surrounding cells 1 Technical 2 | GSM2432255 | tissue:2 000 Inner ear surrounding cells|cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP neg surrounding cells 1 Technical 2 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear surrounding cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432255 | GSM2432255: GFP neg surrounding cells 1 Technical 2; Danio rerio; RNA Seq | GSM2432255 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432255 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | fish_WT_CGTACTAG-_L002_R1_001.fastq.gz | fastq | 2079575456.0 | 20589856.0 | GSM2432255 r1 | 0:101 | A:507789042;C:378574589;G:384399617;T:500198055;N:308614153 | 101 | 507789042 | 378574589 | 384399617 | 500198055 | 308614153 | SRX2435377 | SRS1870364 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.64962 | 0.22792 | 0.76148 | 0.49037 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 41686 | 41686 | SRR5120133 | SRX2435376 | SRS1870363 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP neg surrounding cells 1 Technical 1 | GSM2432254 | tissue:2 000 Inner ear surrounding cells|cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP neg surrounding cells 1 Technical 1 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear surrounding cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432254 | GSM2432254: GFP neg surrounding cells 1 Technical 1; Danio rerio; RNA Seq | GSM2432254 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432254 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | fish_WT_CGTACTAG-_L001_R1_001.fastq.gz | fastq | 2104552049.0 | 20837149.0 | GSM2432254 r1 | 0:101 | A:514445451;C:383531037;G:389222968;T:506643466;N:310709127 | 101 | 514445451 | 383531037 | 389222968 | 506643466 | 310709127 | SRX2435376 | SRS1870363 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.6506 | 0.22936 | 0.76104 | 0.48864 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 41687 | 41687 | SRR5120132 | SRX2435375 | SRS1870362 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP+ Hair Cells Biological Replicate 2 Technical 2 | GSM2432253 | tissue:2 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP+ Hair Cells Biological Replicate 2 Technical 2 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432253 | GSM2432253: GFP+ Hair Cells Biological Replicate 2 Technical 2; Danio rerio; RNA Seq | GSM2432253 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432253 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | zhc_AGGCAGAA-_L002_R1_001.fastq.gz | fastq | 6093457260.0 | 60331260.0 | GSM2432253 r1 | 0:101 | A:1471320441;C:1109536878;G:1119505740;T:1436533942;N:956560259 | 101 | 1471320441 | 1109536878 | 1119505740 | 1436533942 | 956560259 | SRX2435375 | SRS1870362 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.64117 | 0.14727 | 0.78145 | 0.5689 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 41688 | 41688 | SRR5120131 | SRX2435374 | SRS1870361 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP+ Hair Cells Biological Replicate 2 Technical 1 | GSM2432252 | tissue:2 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP+ Hair Cells Biological Replicate 2 Technical 1 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432252 | GSM2432252: GFP+ Hair Cells Biological Replicate 2 Technical 1; Danio rerio; RNA Seq | GSM2432252 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432252 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | zhc_AGGCAGAA-_L001_R1_001.fastq.gz | fastq | 6181180911.0 | 61199811.0 | GSM2432252 r1 | 0:101 | A:1493795643;C:1126661332;G:1135879285;T:1459382790;N:965461861 | 101 | 1493795643 | 1126661332 | 1135879285 | 1459382790 | 965461861 | SRX2435374 | SRS1870361 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.64372 | 0.14904 | 0.78301 | 0.5671 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 41689 | 41689 | SRR5120130 | SRX2435373 | SRS1870360 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP+ Hair Cells Biological Replicate 1 Technical 2 | GSM2432251 | tissue:2 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP+ Hair Cells Biological Replicate 1 Technical 2 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432251 | GSM2432251: GFP+ Hair Cells Biological Replicate 1 Technical 2; Danio rerio; RNA Seq | GSM2432251 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432251 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | fish_TAAGGCGA-_L002_R1_001.fastq.gz | fastq | 1921914355.0 | 19028855.0 | GSM2432251 r1 | 0:101 | A:477226210;C:364711301;G:374540554;T:470661952;N:234774338 | 101 | 477226210 | 364711301 | 374540554 | 470661952 | 234774338 | SRX2435373 | SRS1870360 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.68061 | 0.1576 | 0.7693 | 0.59569 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 41690 | 41690 | SRR5120129 | SRX2435372 | SRS1870359 | SRP095338 | PRJNA358049 | Transcriptomic Analysis of Adult Zebrafish Inner Ear Hair Cells | GSE92559 | Transcriptome Analysis | To understand the basic biological property of hair cells HCs from lower vertebrates we examined transcriptomes of adult zebrafish HCs. GFP labeled HCs were isolated from the utricle saccule and lagena the three inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. 2 000 HCs and 2 000 non sensory cells from the inner ear were individually collected by suction pipet technique. RNA sequencing was performed and the resulting sequences were mapped analyzed and compared. Comparisons allow us to identify enriched genes in HCs which may underlie HC specialization. Overall design: Examination of transcriptomes of adult zebrafish inner ear hair cells and surrounding cells individually collected and sorted using pou4f3 promoter driven GFP marking hair cells. | pubmed:29406519 | GFP+ Hair Cells Biological Replicate 1 Technical 1 | GSM2432250 | tissue:2 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GFP+ Hair Cells Biological Replicate 1 Technical 1 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Expression data was exported from CLC Genomics Workbench in the form of Microsoft Excel Spreadsheets. | 2 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|age:11 mpf 13 mpf adult|Sex:female|strain:Tgpou4f3:GAP GFPs273t | GSM2432250 | GSM2432250: GFP+ Hair Cells Biological Replicate 1 Technical 1; Danio rerio; RNA Seq | GSM2432250 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2432250 | RNA-Seq | TRANSCRIPTOMIC | cDNA | SINGLE | ILLUMINA | Illumina HiSeq 2500 | SRP095338 | fish_TAAGGCGA-_L001_R1_001.fastq.gz | fastq | 1946906300.0 | 19276300.0 | GSM2432250 r1 | 0:101 | A:483944927;C:369830453;G:379601203;T:477313685;N:236216032 | 101 | 483944927 | 369830453 | 379601203 | 477313685 | 236216032 | SRX2435372 | SRS1870359 | SRA505331 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.68178 | 0.1597 | 0.77019 | 0.59655 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2016-12-19 | Adult | Adult | Ear | Sensory System | |||||||||||||||||||
| 42948 | 42948 | SRR5853089 | SRX3022436 | SRS2371721 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP neg Control surrounding cells 3 | GSM2712284 | tissue:1 000 Inner ear surrounding cells|cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP neg Control surrounding cells 3 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear surrounding cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712284 | GSM2712284: GFP neg Control surrounding cells 3; Danio rerio; RNA Seq | GSM2712284 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712284 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFControl3_S3_L001_R1_001.fastq.gz ZFControl3_S3_L001_R2_001.fastq.gz | fastq fastq | 4109673117.0 | 45498619.0 | GSM2712284 r1 | 0:90.33 1:0 | A:1180209080;C:857937316;G:867108081;T:1202304007;N:2114633 | 90 | 0 | 1180209080 | 857937316 | 867108081 | 1202304007 | 2114633 | SRX3022436 | SRS2371721 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.89781 | 0.12518 | 0.74966 | 0.65157 | 40 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System | ||||||||||||||||||
| 42949 | 42949 | SRR5853087 | SRX3022435 | SRS2371720 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP neg Control surrounding cells 2 | GSM2712283 | tissue:1 000 Inner ear surrounding cells|cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP neg Control surrounding cells 2 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear surrounding cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712283 | GSM2712283: GFP neg Control surrounding cells 2; Danio rerio; RNA Seq | GSM2712283 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712283 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFControl2_S2_L001_R1_001.fastq.gz ZFControl2_S2_L001_R2_001.fastq.gz | fastq fastq | 5277482903.0 | 59741039.0 | GSM2712283 r1 | 0:88.34 1:0 | A:1487835111;C:1133268730;G:1145158631;T:1508220719;N:2999712 | 88 | 0 | 1487835111 | 1133268730 | 1145158631 | 1508220719 | 2999712 | SRX3022435 | SRS2371720 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.89608 | 0.11913 | 0.74452 | 0.64488 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System | ||||||||||||||||||
| 42950 | 42950 | SRR5853085 | SRX3022434 | SRS2371718 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP neg Control surrounding cells 1 | GSM2712282 | tissue:1 000 Inner ear surrounding cells|cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP neg Control surrounding cells 1 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear surrounding cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP neg cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712282 | GSM2712282: GFP neg Control surrounding cells 1; Danio rerio; RNA Seq | GSM2712282 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712282 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFControl1_S1_L001_R1_001.fastq.gz ZFControl1_S1_L001_R2_001.fastq.gz | fastq fastq | 4884084264.0 | 54844980.0 | GSM2712282 r1 | 0:89.05 1:0 | A:1416754694;C:1002154600;G:1012874728;T:1449240729;N:3059513 | 89 | 0 | 1416754694 | 1002154600 | 1012874728 | 1449240729 | 3059513 | SRX3022434 | SRS2371718 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.89495 | 0.12873 | 0.74961 | 0.65345 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System | ||||||||||||||||||
| 42951 | 42951 | SRR5853084 | SRX3022433 | SRS2371719 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP+ Zebrafish Hair Cells Biological Replicate 3 | GSM2712281 | tissue:1 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP+ Zebrafish Hair Cells Biological Replicate 3 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712281 | GSM2712281: GFP+ Zebrafish Hair Cells Biological Replicate 3; Danio rerio; RNA Seq | GSM2712281 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712281 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFgfp+3_S6_L001_R2_001.fastq.gz ZFgfp+3_S6_L001_R1_001.fastq.gz | fastq fastq | 4519238829.0 | 50912071.0 | GSM2712281 r1 | 0:88.77 1:0 | A:1293161930;C:955006076;G:967428880;T:1300944329;N:2697614 | 88 | 0 | 1293161930 | 955006076 | 967428880 | 1300944329 | 2697614 | SRX3022433 | SRS2371719 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.92939 | 0.14631 | 0.75485 | 0.53515 | 98 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System | ||||||||||||||||||
| 42952 | 42952 | SRR5853083 | SRX3022432 | SRS2371717 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP+ Zebrafish Hair Cells Biological Replicate 2 | GSM2712280 | tissue:1 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP+ Zebrafish Hair Cells Biological Replicate 2 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712280 | GSM2712280: GFP+ Zebrafish Hair Cells Biological Replicate 2; Danio rerio; RNA Seq | GSM2712280 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712280 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFgfp+2_S5_L001_R1_001.fastq.gz ZFgfp+2_S5_L001_R2_001.fastq.gz | fastq fastq | 9048065761.0 | 100567605.0 | GSM2712280 r1 | 0:89.97 1:0 | A:2534571144;C:1972906517;G:2001215942;T:2534611481;N:4760677 | 89 | 0 | 2534571144 | 1972906517 | 2001215942 | 2534611481 | 4760677 | SRX3022432 | SRS2371717 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.93842 | 0.12913 | 0.75402 | 0.53067 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System | ||||||||||||||||||
| 42953 | 42953 | SRR5853082 | SRX3022431 | SRS2371716 | SRP113243 | PRJNA395227 | RNA sequencing of Adult Zebrafish Inner Ear Hair Cells | GSE101693 | Transcriptome Analysis | To understand the basic biological properties of inner ear hair cells HCs from non mammalian vertebrates we examined the transcriptome of adult zebrafish auditory and vestibular HCs. GFP labeled HCs were isolated from inner ear sensory epithelia of a pou4f3 promoter driven GAP GFP line of transgenic zebrafish. One thousand HCs and 1 000 non sensory surrounding cells nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. Our dataset provides an extensive resource for understanding the molecular mechanisms underlying morphology function and pathology of adult zebrafish HCs. It also establishes a framework for future characterization of the genes expressed in HCs and for the study of HC evolution. Overall design: One thousand HCs and 1 000 nsSCs were separately collected for each biological replicate using the suction pipette technique. RNA sequencing of three biological replicates for the two cell types was performed. The resulting sequenced reads were mapped. Comparisons between HCs and nsSCs allow identification of enriched genes in HCs which may underlie HC specialization. | pubmed:29406519 | GFP+ Zebrafish Hair Cells Biological Replicate 1 | GSM2712279 | tissue:1 000 Inner ear hair cells|cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GFP+ Zebrafish Hair Cells Biological Replicate 1 | CLC Genomics Workbench software CLC bio Waltham MA USA was used to map the reads to the GRCz10 zebrafish genome and generate gene expression values in the normalized form of reads per kilobase of transcript per million mapped reads RPKM values Genome build: GRCz10 zebrafish genome Supplementary files format and content: Excel file of expression data of hair cells and surrounding control cells using RPKM values | 1 000 Inner ear hair cells | Qiagen miRNeasy mini plus kit Clontech Smart Seq | cell type:GFP+ Hair Cells isolated and pooled from the lagena utricle and saccule|passages:11 mpf 13 mpf adult female zebrafish|strain:Tgpou4f3:GAP GFPs273t | GSM2712279 | GSM2712279: GFP+ Zebrafish Hair Cells Biological Replicate 1; Danio rerio; RNA Seq | GSM2712279 | 1 | Qiagen miRNeasy mini plus kit Clontech Smart Seq | GEO Accession:GSM2712279 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2500 | SRP113243 | ZFgfp+1_S4_L001_R1_001.fastq.gz ZFgfp+1_S4_L001_R2_001.fastq.gz | fastq fastq | 1315401262.0 | 14413064.0 | GSM2712279 r1 | 0:91.26 1:0 | A:370914131;C:284206703;G:289196987;T:370556334;N:527107 | 91 | 0 | 370914131 | 284206703 | 289196987 | 370556334 | 527107 | SRX3022431 | SRS2371716 | SRA589592 | GEO | Department of Biomedical Sciences, Creighton University | 1 | 0.93705 | 0.13551 | 0.75471 | 0.53888 | 101 | B | usable mapping rate | illumina | hiseq_era | unknown | cdna_unspecified | unknown | sc | single_cell_plate | smartseq | United States | 2017-07-20 | Adult | Adult | Ear | Sensory System |
Advanced export
JSON shape: default, array, newline-delimited
CREATE TABLE run_metadata("run.accession" VARCHAR, "experiment.accession" VARCHAR, "sample.accession" VARCHAR, "study.accession" VARCHAR, bioproject VARCHAR, "study.title" VARCHAR, "study.alias" VARCHAR, "study.type" VARCHAR, "study.abstract" VARCHAR, "study.attributes" VARCHAR, "study.PMIDs" VARCHAR, "sample.description" VARCHAR, "sample.title" VARCHAR, "sample.alias" VARCHAR, "sample.centername" VARCHAR, "sample.attributes" VARCHAR, "GEOsample.title" VARCHAR, "GEOsample.dataprocessing" VARCHAR, "GEOsample.source" VARCHAR, "GEOsample.treatmentprotocol" VARCHAR, "GEOsample.extractprotocol" VARCHAR, "GEOsample.growthprotocol" VARCHAR, "GEOsample.characteristics" VARCHAR, "GEOsample.accession" VARCHAR, "experiment.title" VARCHAR, "experiment.alias" VARCHAR, "experiment.library_name" VARCHAR, "experiment.design_description" VARCHAR, "experiment.library_construction_protocol" VARCHAR, "experiment.attributes" VARCHAR, "experiment.library_strategy" VARCHAR, "experiment.library_source" VARCHAR, "experiment.library_selection" VARCHAR, "experiment.library_layout" VARCHAR, "experiment.platform" VARCHAR, "experiment.instrument_model" VARCHAR, "experiment.spot_descriptor" VARCHAR, "experiment.study_ref" VARCHAR, "run.title" VARCHAR, "run.attributes" VARCHAR, "run.filename" VARCHAR, "run.semantic_name" VARCHAR, "run.total_bases" DOUBLE, "run.total_spots" DOUBLE, "run.alias" VARCHAR, "run.read_lengths" VARCHAR, "run.base_counts" VARCHAR, "run.r1_length" BIGINT, "run.r2_length" BIGINT, "run.r3_length" BIGINT, "run.r4_length" BIGINT, "run.Acount" BIGINT, "run.Ccount" BIGINT, "run.Gcount" BIGINT, "run.Tcount" BIGINT, "run.Ncount" BIGINT, "run.experiment" VARCHAR, "run.pool_member" VARCHAR, "submission.accession" VARCHAR, "submission.srasource" VARCHAR, "submission.bioprojectsource" VARCHAR, "seqdetective.n_mates" BIGINT, "seqdetective.mapping_rate.mate1" DOUBLE, "seqdetective.mapping_rate.mate2" DOUBLE, "seqdetective.nofeature_rate.mate1" DOUBLE, "seqdetective.nofeature_rate.mate2" DOUBLE, "seqdetective.sparsity.mate1" DOUBLE, "seqdetective.sparsity.mate2" DOUBLE, "seqdetective.pos_strand_rate.mate1" DOUBLE, "seqdetective.pos_strand_rate.mate2" DOUBLE, "seqdetective.readlen.mate1" BIGINT, "seqdetective.readlen.mate2" BIGINT, "seqdetective.judgement.mate1" VARCHAR, "seqdetective.judgement.mate2" VARCHAR, "seqdetective.judgement.reason" VARCHAR, platform_family VARCHAR, instrument_generation VARCHAR, read_bias VARCHAR, selection_class VARCHAR, prep_kit VARCHAR, sc_or_bulk VARCHAR, tech_class VARCHAR, technology VARCHAR, tech_variant VARCHAR, "submission.bioprojectsource.country" VARCHAR, earliest_date DATE, devstage_curation VARCHAR, devstage_curation_coarse VARCHAR, tissue_curation VARCHAR, tissue_curation_coarse VARCHAR);;
CREATE INDEX idx_run_bioproject ON run_metadata(bioproject);;
CREATE INDEX idx_run_run_accession ON run_metadata("run.accession");;