<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE39nnn/GSE39069/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE39069</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Ikaros affects multiple lineages in hematopoietic development [RNA-Seq]</name><description>Ikaros is a zinc finger transcription factor critical for proper hematopoietic development and tumor suppression in the lymphoid lineage. Here, we use the newly generated Ik-ZnF1-/- and Ik-ZnF4-/- mutant mice to study hematopoietic development in the BM. As an initial approach to study early hematopoietic development as well as non-lymphoid lineages, RNA-Seq was performed on "Hardy Fraction A" cells, without lineage depletion (B220+IgM-CD43+CD24-BP-1-), of wt and Ik-ZnF1-/- mice (two biological replicates of each). Ik-ZnF4-/- mice have extremely few cells in the "Hardy fraction A" gate, and only one RNA-Seq experiment was performed on this cell population, with strongly reduced reads/genome coverage.</description><dates><publication>2026/05/30</publication></dates><accession>GSE39069</accession><cross_references><GSM>GSM955180</GSM><GSM>GSM955181</GSM><GSM>GSM955177</GSM><GSM>GSM955178</GSM><GSM>GSM955179</GSM><GPL>13112</GPL><SRA>SRP013993</SRA><GSE>39069</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>