<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/GSE347528/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE347528</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic comparison of colorectal cancer biopsies and human iPSC-derived intestinal organoids</name><description>This bulk RNA-seq study compares primary colorectal cancer and metastatic colorectal cancer biopsy samples, adjacent normal colorectal tissue, and human iPSC-derived intestinal organoids. The dataset supports analysis of transcriptional differences in epithelial lineage identity, inflammatory and stromal remodeling, extracellular matrix organization, metabolic adaptation, and tissue-level regulatory programs.</description><dates><publication>2026/09/17</publication></dates><accession>GSE347528</accession><cross_references><GSM>GSM10054750</GSM><GSM>GSM10054743</GSM><GSM>GSM10054742</GSM><GSM>GSM10054752</GSM><GSM>GSM10054741</GSM><GSM>GSM10054740</GSM><GSM>GSM10054751</GSM><GSM>GSM10054747</GSM><GSM>GSM10054736</GSM><GSM>GSM10054735</GSM><GSM>GSM10054746</GSM><GSM>GSM10054745</GSM><GSM>GSM10054734</GSM><GSM>GSM10054744</GSM><GSM>GSM10054733</GSM><GSM>GSM10054739</GSM><GSM>GSM10054738</GSM><GSM>GSM10054749</GSM><GSM>GSM10054737</GSM><GSM>GSM10054748</GSM><GPL>24676</GPL><GPL>29480</GPL><GSE>347528</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>