<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/GSE249nnn/GSE249305/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></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=GSE249305</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single cell analysis of human peripheral blood cells</name><description>In this study, we aimed to identify human T cell clonotypes ractive to tumor-associated metabolites. For this purpose, we generated tumors that lack a particular metabolite. After the tumor was cocultured with human peripheral blood mononuclear cells, proliferated cells were sorted and applied for single cell analysis. We identified 17 T cell clonotypes that underwent clonal expansion.</description><dates><publication>2026/06/15</publication></dates><accession>GSE249305</accession><cross_references><GSM>GSM7933326</GSM><GSM>GSM7933327</GSM><GPL>28038</GPL><GSE>249305</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>