<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/GSE277nnn/GSE277496/</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> Genome binding/occupancy profiling by high throughput sequencing</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=GSE277496</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Single-cell multiomics of peripheral blood monocytes in Crohn's Disease</name><description>Dysfunctional intestinal monocyte-derived macrophages contribute to pathology in Inflammatory Bowel Disease (IBD). Signals from the tissue micro-environment contribute to this dysfunction, however growing evidence suggests that monocytes can be primed for inflammatory function prior to tissue recruitment. Here we use single-nucleus multiomics, comprising RNA sequencing (RNA-seq) and assay for transposase-accessible chromatin using sequencing (ATAC-seq) to identify regulatory elements underlying the altered transcriptional profile in monocytes from newly diagnosed, treatment naive Crohn’s disease patients.</description><dates><publication>2026/07/23</publication></dates><accession>GSE277496</accession><cross_references><GSM>GSM8523383</GSM><GSM>GSM8523382</GSM><GSM>GSM8523381</GSM><GSM>GSM8523380</GSM><GSM>GSM8523379</GSM><GSM>GSM8523378</GSM><GSM>GSM8523377</GSM><GSM>GSM8523387</GSM><GSM>GSM8523376</GSM><GSM>GSM8523386</GSM><GSM>GSM8523385</GSM><GSM>GSM8523384</GSM><GPL>30173</GPL><GSE>277496</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>