<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Txt>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/suppl/filelist.txt</Txt><Raw>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/suppl/GSE315817_RAW.tar</Raw><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Sus scrofa</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=GSE315817</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Dynamic Cellular Heterogeneity Revealed through a Time-Resolved Single-Cell Atlas in porcine intestinal organoids</name><description>Intestinal epithelial cells are supported by dynamic cellular heterogeneity, which is critical for maintaining intestinal homeostasis. Recently, intestinal organoid models have been attracting in-vitro platform because they can recapitulate the structural, functional, and cellular complexity of the small intestine. Here, we established porcine intestinal organoids and investigated time-dependent transcriptomic changes using single-cell RNA sequencing.</description><dates><publication>2026/06/10</publication></dates><accession>GSE315817</accession><cross_references><GSM>GSM9437894</GSM><GSM>GSM9437895</GSM><GSM>GSM9437896</GSM><GPL>26351</GPL><GSE>315817</GSE><taxon>Sus scrofa</taxon><PMID>[42231404]</PMID></cross_references></HashMap>