<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/GSE335nnn/GSE335246/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE335246</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Differential chromatin accessability in follicular B cells, marginal zone B cells and newly formed plasma cells. [ATAC-Seq]</name><description>Marginal zozne B cells are poised to rapidly differentiate into plasma cells through biochemical pathways activated by Notch2 signaling. We sought to determine differences in chromatin accessability at plasma cell program-relevant loci between these cells and follicular B cells also located within the spleen but less receptive to Notch signaling. To ths end, we prepared ATAC-seq libriaries from steady state marginal zone and follicular B cells as well as newly formed plasma cells generated in Blimp1GFP/+ reporter mice 4 days post immunization with LPS.</description><dates><publication>2026/07/08</publication></dates><accession>GSE335246</accession><cross_references><GSM>GSM9808981</GSM><GSM>GSM9808982</GSM><GSM>GSM9808980</GSM><GSM>GSM9808974</GSM><GSM>GSM9808975</GSM><GSM>GSM9808983</GSM><GSM>GSM9808972</GSM><GSM>GSM9808973</GSM><GSM>GSM9808978</GSM><GSM>GSM9808979</GSM><GSM>GSM9808976</GSM><GSM>GSM9808977</GSM><GPL>19057</GPL><GSE>335246</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>