<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/GSE347nnn/GSE347847/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE347847</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell ATAC-seq profiling of ARID1A-loss-associated chromatin accessibility heterogeneity in pancreatic cancer cells</name><description>This Series contains single-cell ATAC-seq datasets from clone-resolved and pooled perturbation experiments examining how ARID1A and other epigenetic modifiers influence chromatin-accessibility heterogeneity in pancreatic ductal adenocarcinoma cells. The datasets include the main 28-clone BxPC3 experiment, a large-scale pooled five-shRNA experiment, acute SMARCA4 degradation with AU-15330, and independent experiments in BxPC3, HPAC/HPAFII, SW1990, and SUIT-2 backgrounds. PseuMO-Tag lineage barcodes were used to connect single-cell chromatin profiles to clonal identity.</description><dates><publication>2026/09/22</publication></dates><accession>GSE347847</accession><cross_references><GSM>GSM10061726</GSM><GSM>GSM10061727</GSM><GSM>GSM10061728</GSM><GSM>GSM10061729</GSM><GSM>GSM10061719</GSM><GSM>GSM10061730</GSM><GSM>GSM10061731</GSM><GSM>GSM10061720</GSM><GSM>GSM10061732</GSM><GSM>GSM10061721</GSM><GSM>GSM10061733</GSM><GSM>GSM10061722</GSM><GSM>GSM10061723</GSM><GSM>GSM10061724</GSM><GSM>GSM10061725</GSM><GPL>21697</GPL><GSE>347847</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>