<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/GSE218nnn/GSE218337/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE218337</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Genotype-phenotype relationships (VPA/CHIR99021 vs. control; p53 Null vs. WT) in bulk RNA-sequencing of small intestinal murine organoids [bulk RNA-seq]</name><description>WT and Trp53 knock-out small intestinal organoids were cultured in standard ENR medium or treated with VPA and CHIR99021 for 5 days. At the endpoint of the culture, RNA was extracted from the cells and analysed with paired-end RNA-sequencing.</description><dates><publication>2026/06/01</publication></dates><accession>GSE218337</accession><cross_references><GSM>GSM6742591</GSM><GSM>GSM6742592</GSM><GSM>GSM6742593</GSM><GSM>GSM6742602</GSM><GSM>GSM6742603</GSM><GSM>GSM6742604</GSM><GSM>GSM6742605</GSM><GSM>GSM6742606</GSM><GSM>GSM6742607</GSM><GSM>GSM6742594</GSM><GSM>GSM6742595</GSM><GSM>GSM6742596</GSM><GSM>GSM6742597</GSM><GSM>GSM6742598</GSM><GSM>GSM6742599</GSM><GSM>GSM6742600</GSM><GSM>GSM6742601</GSM><GPL>17021</GPL><GSE>218337</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>