<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/GSE316nnn/GSE316206/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</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=GSE316206</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Impact of Mettl1 on the transcriptional landscape of mouse bone marrow cells at single-cell resolution [scRNA-seq]</name><description>This study investigates the impact of Mettl1 deletion on the transcriptional landscape of bone marrow cells at single-cell resolution. Bone marrow mononuclear cells (BM MNCs) were collected from Mettl1+/+ Mx1-Cre and Mettl1fl/fl Mx1-Cre mice following poly(I:C)-induced recombination. Single-cell RNA sequencing (scRNA-seq) was performed using the 10x Genomics Chromium platform. The resulting data were used to identify distinct cell populations, and assess transcriptional changes associated with Mettl1 loss. This dataset provides a valuable resource for understanding the role of Mettl1 in normal hematopoiesis.</description><dates><publication>2026/07/29</publication></dates><accession>GSE316206</accession><cross_references><GSM>GSM9447351</GSM><GSM>GSM9447352</GSM><GPL>34328</GPL><GSE>316206</GSE><taxon>Mus musculus</taxon><PMID>[42247311]</PMID></cross_references></HashMap>