<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/GSE304nnn/GSE304943/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE304943</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>TET2 drives myeloid cell fate acquisition through AGO2 modulation [ChIP-seq, TET2]</name><description>We determined TET2 genome-wide occupancy through FLAG-tag based capturing during C/EBPa-driven transdifferentiation of B-cells into iMacs</description><dates><publication>2026/07/09</publication></dates><accession>GSE304943</accession><cross_references><GSM>GSM9160017</GSM><GSM>GSM9160016</GSM><GSM>GSM9160019</GSM><GSM>GSM9160018</GSM><GPL>28038</GPL><GSE>304943</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>