<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/GSE299nnn/GSE299458/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Methylation profiling</omics_type><species>Mus musculus</species><gds_type>Methylation profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE299458</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Methylome profiling of SetDB1 deficient ESCs reveals coordinated epigenetic cross-talk during pluripotency</name><description>DNA methylation profiling using whole-genome bisulfite sequencing of conditional SetDB1 knockout (KO) mouse embryonic stem cells (ESCs). Induction with 4-hydroxytamoxifen (4-OHT) facilitated the deletion of Setdb1 floxed exons 15 and 16, resulting in loss of SetDB1. Methylomes were profiled in wildtype (WT) serum- and 2i-cultured ESCs, and on multiple days after inducing SetDB1 depletion. Study also includes methylome profiles of ESCs undergoing simultaneous SetDB1 depletion and 2i-adaptation.</description><dates><publication>2026/06/10</publication></dates><accession>GSE299458</accession><cross_references><GSM>GSM9039479</GSM><GSM>GSM9039477</GSM><GSM>GSM9039478</GSM><GSM>GSM9039475</GSM><GSM>GSM9039476</GSM><GSM>GSM9039484</GSM><GSM>GSM9039473</GSM><GSM>GSM9039485</GSM><GSM>GSM9039474</GSM><GSM>GSM9039482</GSM><GSM>GSM9039483</GSM><GSM>GSM9039480</GSM><GSM>GSM9039481</GSM><GPL>13112</GPL><GSE>299458</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>