{"database":"GEO","file_versions":[{"headers":{"Content-Type":["application/json"]},"body":{"files":{"Txt":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/suppl/filelist.txt"],"Raw":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/suppl/GSE315817_RAW.tar"],"Other":["ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE315nnn/GSE315817/"]},"type":"primary"},"statusCode":"OK","statusCodeValue":200}],"scores":null,"additional":{"omics_type":["Transcriptomics"],"species":["Sus scrofa"],"gds_type":["Expression profiling by high throughput sequencing"],"full_dataset_link":["https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE315817"],"repository":["GEO"],"entry_type":["GSE"],"additional_accession":[]},"is_claimable":false,"name":"Dynamic Cellular Heterogeneity Revealed through a Time-Resolved Single-Cell Atlas in porcine intestinal organoids","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.","dates":{"publication":"2026/06/10"},"accession":"GSE315817","cross_references":{"GSM":["GSM9437894","GSM9437895","GSM9437896"],"GPL":["26351"],"GSE":["315817"],"taxon":["Sus scrofa"],"PMID":["[42231404]"]}}