<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/GSE305nnn/GSE305118/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</species><gds_type> Other</gds_type><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE305118</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Pro-inflammatory role of granzyme K producing bystander CD8 T cells in acute myeloid leukemia</name><description>This study investigates the composition, antigen specificity, and functional characteristics of CD8⁺ T cells in acute myeloid leukemia (AML). Using paired blood and bone marrow samples from AML patients, we performed single-cell transcriptomic (CITE-seq) and T cell receptor (VDJ) profiling to identify immune cell subsets and their clonotypes.</description><dates><publication>2026/08/10</publication></dates><accession>GSE305118</accession><cross_references><GSM>GSM9162471</GSM><GSM>GSM9162470</GSM><GSM>GSM9162473</GSM><GSM>GSM9162462</GSM><GSM>GSM9162472</GSM><GSM>GSM9162464</GSM><GSM>GSM9162475</GSM><GSM>GSM9162463</GSM><GSM>GSM9162474</GSM><GSM>GSM9162466</GSM><GSM>GSM9162476</GSM><GSM>GSM9162465</GSM><GSM>GSM9162468</GSM><GSM>GSM9162467</GSM><GSM>GSM9162469</GSM><GPL>18573</GPL><GSE>305118</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>