<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/GSE293nnn/GSE293758/</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> 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=GSE293758</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Spatial and Functional Specialization of Human Splenic Innate Lymphoid Cells (CITE-seq]</name><description>To date, the spatial and functional characterization of human splenic innate lymphoid cells (ILC) has remained limited. Here, the authors integrate CITE-seq and spatial transcriptomic data and present an atlas of human splenic NK and ILC cells, and define high-resolution subset-specific spatial organization and interaction networks, providing insights into the presence of local immune niches in secondary lymphoid organs.</description><dates><publication>2026/05/06</publication></dates><accession>GSE293758</accession><cross_references><GSM>GSM8889634</GSM><GSM>GSM8889633</GSM><GSM>GSM8889636</GSM><GSM>GSM8889635</GSM><GSM>GSM8889641</GSM><GSM>GSM8889640</GSM><GSM>GSM8889632</GSM><GSM>GSM8889638</GSM><GSM>GSM8889637</GSM><GSM>GSM8889639</GSM><GPL>24676</GPL><GSE>293758</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>