{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE348nnn/GSE348238/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Genomics"],"species":["Homo sapiens"],"gds_type":["Genome binding/occupancy profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE348238"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"SMARCA4 CUT&Tag profiling in parental and ARID1A-knockdown BxPC3 pancreatic cancer clones","description":"This Series profiles SMARCA4 (BRG1) chromatin occupancy by CUT&Tag in parental BxPC3 pancreatic ductal adenocarcinoma cells and selected control or ARID1A-knockdown clonal populations. The data were generated to examine whether residual SMARCA4 preferentially occupies regulatory regions associated with increased and variable chromatin accessibility after ARID1A loss. Drosophila spike-in nuclei were included for quantitative normalization.","dates":{"publication":"2026/09/22"},"accession":"GSE348238","cross_references":{"GSM":["GSM10068926","GSM10068925","GSM10068929","GSM10068928","GSM10068927"],"GPL":["21697"],"GSE":["348238"],"taxon":["Homo sapiens"]}}