<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>University of Toronto</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1167332</full_dataset_link><scientific_name>Homo sapiens</scientific_name><tag>xref:PubMed:40604231</tag><long_description>Pancreatic ductal adenocarcinoma is a high-mortality cancer with an aggressive, treatment resistant phenotype and a complex tumour microenvironment featuring significant hypoxia. We leveraged a unique 3D in vitro platform (TRACER) to perform single-cell transcriptome analysis of organoids cultured in a spatially-defined microenvironmental gradient to explore the effect of oxygen and other microenvironmental gradients on organoid heterogeneity. Overall design: Pancreatic cancer patient-derived organoids (PDOs) were dissociated to single cells and cultured in the TRACER platform. After 24h of culture in the rolled configuration featuring microenvironmental gradients, cells from each of the 6 layers were isolated from the construct and analyzed by scRNA-seq.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Single cell analysis of an engineered organoid based model of pancreatic cancer identifies hypoxia as a contributing factor in the determination of transcriptional subtypes</name><description>Single cell analysis of an engineered organoid based model of pancreatic cancer identifies hypoxia as a contributing factor in the determination of transcriptional subtypes</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-07-17</first_public></dates><accession>PRJNA1167332</accession><cross_references><GEO>GSE278477</GEO><taxon>9606</taxon><PubMed>40604231</PubMed></cross_references></HashMap>