ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/007/SRR5331877/SRR5331877.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/008/SRR5331878/SRR5331878.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/001/SRR5331881/SRR5331881.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/000/SRR5331880/SRR5331880.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/009/SRR5331879/SRR5331879.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR533/002/SRR5331882/SRR5331882.fastq.gzprimaryOK200GenomicsBresnick lab, Cell and Regenerative Biology, University of Wisconsin Madisonhttps://www.ebi.ac.uk/ena/browser/view/PRJNA378680Mus musculusGene expression profiles of sorted erythroid precursors from E14.5 wild-type (WT) and -77 enhancer knockout (-77-/-) mouse fetal liver were generated by next generation sequencing, in triplicate, using Illumina Hiseq2500 (1X50). We showed that the Gata2 -77 enhancer generated the vital erythroid precursor Burst Forming Unit-Erythroid by two mechanisms, GATA-1 upregulation to establish the erythroid transcriptome and GATA-2-dependent, GATA-1-independent transcriptional regulation. Overall design: Erythroid precursor gene expression profiles of E14.5 mouse -77+/+ and -77-/- mouse fetal livers were generated by next generation sequencing, in triplicate, using Illumina Hiseq2500 (1X50).xref:PubMed:28930689ENAfalseMus musculusNext Generation sequencing and quantitative transcriptomic analysis in -77+/+ and -77-/- erythroid precursors2025-09-242017-09-20PRJNA378680GSE960591009028930689