<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/GSE327nnn/GSE327306/</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=GSE327306</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>DOT1L shapes ncPRC1-target gene repression to maintain cell identity of DLBCL [CUT&amp;Tag]</name><description>DOT1L inhibition leads to a loss of H2AK119ub1 in different GC B-DLBCL cell lines. To determine whether this loss is global or gene specific, performed H2AK119ub1 and H3K27me3 CUT&amp;Tag in the Oci-Ly7 cell line following six days of treatment with DMSO or DOT1Li. As reference, we used a doxycycline-inducible knockdown of USP7 due to its role in ncPRC1-mediated deposition of H2AK119ub1 in Oci-Ly7 cells.</description><dates><publication>2026/06/19</publication></dates><accession>GSE327306</accession><cross_references><GSM>GSM9653198</GSM><GSM>GSM9653199</GSM><GSM>GSM9653200</GSM><GSM>GSM9653201</GSM><GSM>GSM9653194</GSM><GSM>GSM9653195</GSM><GSM>GSM9653196</GSM><GSM>GSM9653197</GSM><GSM>GSM9653191</GSM><GSM>GSM9653192</GSM><GSM>GSM9653193</GSM><GSM>GSM9653202</GSM><GPL>18573</GPL><GSE>327306</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>