<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/GSE295nnn/GSE295989/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Other</omics_type><species>Mus musculus</species><gds_type> Expression profiling by high throughput sequencing</gds_type><gds_type>Other</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE295989</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Bulk B Cell Receptor Sequencing of mouse ileum; paired sample with MERFISH imaging</name><description>Plasma B cell clones each express a single B cell receptor that has high binding specificity to a narrow set of antigens. New spatial technologies have been introduced that aim to capture the clonality of plasma cell populations in situ. BCR-MERFISH is an imaging- and probe-based spatial approach that targets the V genes of heavy and light chains that comprise B cell receptors within single cells. To assess how accurately BCR-MERFISH reports V gene usage, this BCR-sequencing dataset was collected from paired samples that were imaged with BCR-MERFISH.</description><dates><publication>2026/08/18</publication></dates><accession>GSE295989</accession><cross_references><GSM>GSM9538669</GSM><GSM>GSM8962912</GSM><GPL>16417</GPL><GSE>295989</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>