run_metadata: 59880
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| 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 |
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| 59880 | SRR12060554 | SRX8588729 | SRS6880197 | SRP268145 | PRJNA640816 | An atlas of neural crest lineages along the posterior developing zebrafish at single cell resolution | GSE152906 | Transcriptome Analysis | Neural crest cells NCCs are vertebrate stem cells that give rise to various cell types throughout the developing body in early life. Here we utilized single cell transcriptomic analyses to delineate NCC derivatives along the posterior developing vertebrate zebrafish during the late embryonic to early larval stage a period when NCCs are actively differentiating into distinct cellular lineages. We identified several major NCC/NCC derived cell types including mesenchyme neural crest neural neuronal glial and pigment from which we resolved over three dozen cellular subtypes. We dissected gene expression signatures of pigment progenitors delineating into chromatophore lineages mesenchyme subtypes and enteric NCCs transforming into enteric neurons. Global analysis of NCC derivatives revealed they were demarcated by combinatorial hox gene codes with distinct profiles within neuronal cells. From these analyses we present a comprehensive cell type atlas that can be utilized as a valuable resource for further mechanistic and evolutionary investigations of NCC differentiation. Overall design: To characterize the neural crest cell lineages present in the posterior zebrafish during the embryonic to larval transition 48 hpf 72 hpf we utilized single cell RNA sequencing scRNA Seq on the 10x Genomics Chromium platform to build a dataset from GFP+ cells collected from sox10:GFP embryos. | pubmed:33591267;pubmed:38234831;pubmed:38809858 | Sox10+ 68 70hpf | GSM4629199 | tissue:Derivative Sox10+ Neural Crest|genotype/variation: 4.9sox10:EGFP ba2Tg|developmental stage:68 hpf 70 hpf|cell type:FACS isolated 4.9sox10:EGFP+ cells | Sox10+ 68 70hpf | Illumina NextSeq 500 used for basecalling CellRanger v2.1.0 software facilitated genomic alignment filtering barcode reading and exportation for further analysis Genome build: DanioGRCz10 Supplementary files format and content: 10X Genomics Chromim Filtered Gene BC Cellular Barcodes barcodes.tsv and genes genes.tsv; 10X Genomics Chromium Raw Gene BC Cellular Matrix matrix.mtx | Derivative Sox10+ Neural Crest | none | Posterior tissue Vagal and trunk domains were harvested; Single cell suspension was prepared via digestion in 37°C 1X Accumax buffer Sigma Aldrich A7089 for 30 45 minutes. Suspension was washed in Hank's Buffer 1x HBSS; 2.5 mg/mL BSA; 10μM pH8 HEPES concentrated via centrifugation 200 rcf for 10 minutes at 4°C in a small volume of Hank's buffer and sorted for GFP+ cells via FACS. GFP+ cells were used as input for the 10X Genomics Chromium platform using the 10X Single Cell 3’ V2 chemistry kit for 10 000 cells. RNA libraries were prepared for sequencing using standard Illumina protocols following the 10x Genomics pipeline | Embryos were collected synchronously batched by stage. All embryos were raised according to standard practices in E3 embryonic media for the first 24 hours and then transfered to 1X 1 phenyl 2 thiourea PTU/E3 solution. At 24 hpf embryos were sorted manually for GFP expression. Developmentally delayed or malformed embryos were removed. All work was conducted under protocols approved by and in accordance with Rice University Institutional Animal Care and Use Committee IACUC. | genotype/variation: 4.9sox10:EGFP ba2Tg|developmental stage:68 hpf 70 hpf|cell type:FACS isolated 4.9sox10:EGFP+ cells | GSM4629199 | GSM4629199: Sox10+ 68 70hpf; Danio rerio; RNA Seq | GSM4629199 | 1 | Posterior tissue Vagal and trunk domains were harvested; Single cell suspension was prepared via digestion in 37°C 1X Accumax buffer Sigma Aldrich A7089 for 30 45 minutes. Suspension was washed in Hank's Buffer 1x HBSS; 2.5 mg/mL BSA; 10μM pH8 HEPES concentrated via centrifugation 200 rcf for 10 minutes at 4°C in a small volume of Hank's buffer and sorted for GFP+ cells via FACS. GFP+ cells were used as input for the 10X Genomics Chromium platform using the 10X Single Cell three prime V2 chemistry kit for 10 000 cells. RNA libraries were prepared for sequencing using standard Illumina protocols following the 10x Genomics pipeline | GEO Accession:GSM4629199 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | NextSeq 500 | SRP268145 | loader:fastq load.py|options: platform=Illumina readTypes=BBT read1PairFiles=GFPplus S1 L002 R1 001.fastq read2PairFiles=GFPplus S1 L002 R2 001.fastq read3PairFiles=GFPplus S1 L002 I1 001.fastq | 3615497884.0 | 22882898.0 | GSM4629199 r2 | 0:26 1:124 2:8 | A:1062722875;C:724671651;G:825496420;T:1002262450;N:344488 | 26 | 124 | 8 | 1062722875 | 724671651 | 825496420 | 1002262450 | 344488 | SRX8588729 | SRS6880197 | SRA1089349 | GEO | The Uribe Laboratory, BioSciences, Rice University | 2 | 0.00228 | 0.91709 | 0.00071 | 0.08087 | 0.99557 | 0.80984 | 0.37288 | 0.50652 | 26 | 124 | T | B | sc-like readlen | illumina | nextseq | unknown | cdna_unspecified | unknown | sc | single_cell_droplet | 10x | United States | 2020-06-20 | Hatching | Embryo | Brain | Nervous System |