run_metadata: 64472
This data as json
| 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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| 64472 | SRR14710792 | SRX11048791 | SRS9116826 | SRP322308 | PRJNA734487 | polyA+ RNA seq of zebrafish gonad at 25 dpf and 30dpf | GSE175979 | Transcriptome Analysis | In this study we explored the biological process of zebrafish gonad differentiation through PolyA enriched RNA sequencing and found that the differences in the gonads differentiating towards testis or ovary were represented through types and expression levels of different genes. Using the GO enrichment classification it is found that in the differentiating ovary the differentially expressed genes are enriched in processes of material synthesis and metabolic pathway indicating that oocyte requires the accumulation of maternal RNA protein sugar lipids vitamins and other substances which is consistent with its basic function of providing primary materials for early development of fertilized embryo. In addition during ovarian differentiation the biological processes associated with the nucleus mitochondria and cytoplasmic particles are more active and the genes associated with sperm egg recognition are also expressed during this period. Unlike the differentiating ovary when the gonad differentiates into testis the differentially expressed genes are more enriched in biological regulation and development processes including morphogenesis cell proliferation etc.The cytometers adapted to these biological processes are associated with cell membrane such as membrane receptors extra cellular regions extra cellular matrix and cell connections and also associated with nuclear chromatin. In addition we enriched 14 signaling pathways involved in testis differentiation and showed the expression heat map of every differentially expressed gene of each pathway. Overall the study reveals the different biological processes existing in the differentiation of the zebrafish gonads into ovary or testis helping us to get a comprehensive understanding of the basis on biological events and molecules during this process. Overall design: Zebrafish larvae were anesthetized in 0.2 mg/mL MS 222 and disected to isolate gonads. Each gonad is placed under a microscope to identify either the testis or the ovary. Six 25 dpf and six 30 dpf undamaged gonads with sound integrity were choosen for PolyA+ RNA sequencing. | pubmed:36257818 | 30dpf testis rep2 | GSM5352295 | source name:Gonad|strain:AB|tissue:testis|age:post fertilization day 30|genotype:Tgpiwil1 egfp nos3UTRihb327Tg | 30dpf testis rep2 | High throughput sequencing raw image data files were converted to reads using fqtools plus analysis and using FastqC v0.11.8 and sequencing report tool of MultiQC v0.9to evaluate the raw read quality statistics. Reads were mapped to the corresponding reference genome Ensembl v96 with the parameters " dta x rna strandness RF" and " known spliceset infile" using Hisat2 v2.0.5 and gene annotation was performed in GTF format Ensembl 96. Hisat2 converts the data into BAM format sorted by Samtools v1.5 and removed duplicates using the Picard MarkDuplicates v2.18.15 tool. HTSeq v0.9.1 was used to read and count the parameter " t exon i gene id r pos s reverse". Genome build: GRCz11 Supplementary files format and content: Matrix table with raw gene counts for every gene and every sample | Gonad | Gonads were removed and RNA was extracted using RNAprep pure Micro Kit TIANGEN. For each sample 5ul of RNA was used for synthesis and amplification of cDNA Discover sc WTA Kit N711 Vazyme and 5ng of amplified cDNA was used for construction of sequencing library using TruePrep DNA Library Prep Kit V2 for Illumina® Vazyme TD501/TD502. | The zebrafish were maintained raised and staged according to zebrafish book. The rearing density is 50 larvae/L for age from 5 dpf to 15 dpf 20 fish/L for age 15 dpf to 1 mpf. | strain:AB|tissue:testis|age:post fertilization day 30|genotype:Tgpiwil1 egfp nos3UTRihb327Tg | GSM5352295 | GSM5352295: 30dpf testis rep2; Danio rerio; RNA Seq | GSM5352295 | 1 | Gonads were removed and RNA was extracted using RNAprep pure Micro Kit TIANGEN. For each sample 5ul of RNA was used for synthesis and amplification of cDNA Discover sc WTA Kit N711 Vazyme and 5ng of amplified cDNA was used for construction of sequencing library using TruePrep DNA Library Prep Kit V2 for Illumina® Vazyme TD501/TD502. | GEO Accession:GSM5352295 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | ILLUMINA | Illumina HiSeq 2000 | SRP322308 | 30d_small_2_r1.fastq.gz 30d_small_2_r2.fastq.gz | fastq fastq | 6853411125.0 | 23219079.0 | GSM5352295 r1 | 0:148.28 1:146.88 | A:1858128706;C:1569075657;G:1580228791;T:1845965296;N:12675 | 148 | 146 | 1858128706 | 1569075657 | 1580228791 | 1845965296 | 12675 | SRX11048791 | SRS9116826 | SRA1239593 | GEO | College of Life Science and Technology, Huazhong Agricultural University | 2 | 0.93587 | 0.93627 | 0.05854 | 0.05886 | 0.68081 | 0.68337 | 0.49214 | 0.49713 | 150 | 149 | B | B | biological fallback assumption | illumina | hiseq_era | unknown | poly_a | unknown | bulk | unknown | unknown | China | 2021-06-02 | Juvenile | Juvenile | Gonad | Reproductive System |