<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/GSE295nnn/GSE295009/</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=GSE295009</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Epigenomic analysis of organoids from colorectal cancer peritoneal metastases uncovers a mechanism of resistance to doxorubicin</name><description>In this study, we generated patient-derived organoids (PDOs) from patients with colorectal cancer peritoneal mestasis and performed RNA- and ATAC-sequencing to study mechanisms for doxorubicin response.</description><dates><publication>2026/06/16</publication></dates><accession>GSE295009</accession><cross_references><GSM>GSM8940050</GSM><GSM>GSM8940051</GSM><GSM>GSM8940047</GSM><GSM>GSM8940046</GSM><GSM>GSM8940049</GSM><GSM>GSM8940048</GSM><GSM>GSM8940043</GSM><GSM>GSM8940045</GSM><GSM>GSM8940044</GSM><GPL>24676</GPL><GSE>295009</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>