run_metadata: 55377
This data as json
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| 55377 | SRR10322137 | SRX7032948 | SRS5553008 | SRP226571 | PRJNA578840 | RNA seq analysis for zebrafish tumors driven by overexpression of human IRF4 | GSE139226 | Transcriptome Analysis | RNA seq analysis was performed using zebrafish primary tumors and control thymus to analyze gene expression changes post IRF4 overexpression. Overall design: Human IRF4 gene was overexpressed under the zebrafish lck promoter. Tumor cells were harvested from IRF4 transgenic zebrafish lck IRF4 with or without xxx p53 mutation. Normal thymus cells were also harvested from control zebrafish lck mCherry. | pubmed:35504924 | mCherry control RNA seq #2 | GSM4134347 | tissue:lck mCherry|genotype/variation:control | mCherry control RNA seq #2 | RNA seq datasets of two control thymus samples and four tumor samples two from lck:IRF4 and two from lRF4;p53+/ were aligned to the zebrafish genome GRCz11 using STAR 2.5.2a with the parameter outFilterMultimapNmax set to 1. featureCount v1.6.1 was used for the mapped reads in .bam files to generate count tables based on the Ensembl gene annotation GRCz11 gtf file Bioconductor package DESeq2 v1.12.4 with the intersection strict mode was used to analyze differential gene expression. Genome build: GRCz11 Supplementary files format and content: txt files for raw counts differentially expressed genes | lck mCherry | No treatment | Total RNA was harvested using the Qiagen miRNeasy kit. Strand specific library construction and sequencing of paired end 100 bp long reads by the BGISeq500 were performed at the BGI Biotech Solutions Hong Kong Co Ltd Hong Kong. | The human IRF4 gene and mCherry fluorescent marker gene were transduced under the zebrafish lck promoter in zebrafish. post the development of lymphoma phenotype tumor cells were harvested and sorted by flow cytometry based on mCherry fluorescence expression. Normal thymus were also harvested from control zebrafish which was transduced only with mCherry. Total RNAs were harvested from each sample and then applied for RNA seq analysis. | genotype/variation:control | GSM4134347 | GSM4134347: mCherry control RNA seq #2; Danio rerio; RNA Seq | GSM4134347 | 1 | Total RNA was harvested using the Qiagen miRNeasy kit. Strand specific library construction and sequencing of paired end 100 bp long reads by the BGISeq500 were performed at the BGI Biotech Solutions Hong Kong Co Ltd Hong Kong. | GEO Accession:GSM4134347 | RNA-Seq | TRANSCRIPTOMIC | cDNA | PAIRED | BGISEQ | BGISEQ-500 | SRP226571 | Lck_mch_2_1.fastq.gz Lck_mch_2_2.fastq.gz | fastq fastq | 8556568306.0 | 85629202.0 | GSM4134347 r1 | 0:99.93 1:99.93 | A:2299427498;C:1945648999;G:1981590842;T:2329900967;N:0 | 99 | 99 | 2299427498 | 1945648999 | 1981590842 | 2329900967 | 0 | SRX7032948 | SRS5553008 | SRA982884 | GEO | Takaomi Sanda Lab, Cancer Science Institute, National University of Singapore | 1 | 0.94792 | 0.25274 | 0.80085 | 0.51772 | 100 | B | usable mapping rate | bgi | bgi | unknown | cdna_unspecified | unknown | bulk | unknown | unknown | Singapore | 2019-10-22 | Undetermined | Undetermined | Multi-tissue | Multi-system |