<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>YANG JIANG</submitter><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>ATAC-seq</study_type><organism>Mus musculus</organism><species>Mus musculus</species><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-12903</full_dataset_link><description>To test the chromatin accessibility of different immune cell subsets, we isolated naive B cells CD11c+T-bet+ B cells,  CD11c-T-bet- B cells by flow cytometry from Bm12-induced lupus T-bet reporter mice and performed ATAC assay.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Fragmented DNA was purified using VAHTS DNA Clean Beads and library was generated by PCR.</sample_protocol><sample_protocol>Sample Collection - bm12-cGVHD lupus model was induced following JOVE protocol. Briefly, 8-12-week-old mice were intraperitoneally injected with 10 million CD4+ T cells from bm12 mice purified by magnetic cell sorting and mice were sacrificed for analysis after 2 weeks. Single cell suspensions of splenocytes from Bm12-induced lupus T-bet reporter mice were subjected to red blood cell lysis and filtered through 70 um nylon mesh.Cells were stained for surface markers under instructions. DP and DN B cells were collected through flow cytometry.</sample_protocol><sample_protocol>Sequencing - Illumina HiSeq X Ten</sample_protocol><sample_protocol>Nucleic Acid Extraction - Briefly, 50,000 live cells were freshly isolated and resuspended in lysis buffer (10 mM Tris·Cl,（pH 7.4）,10 mM NaCl，3 mM MgCl2，0.1% (v/v) Igepal CA-630) and pelleted. The cell pellet was resuspended in transposase reaction mix (5×TTBL 10μl, TTE Mix V50 5μl, ddH2O 35μl) and incubated at 37°C for 30 min.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><pubmed_authors>YANG JIANG</pubmed_authors><pubmed_authors>Nan Shen</pubmed_authors></additional><is_claimable>false</is_claimable><name>ATAC-seq in naive B cells, CD11c+T-bet+ B cells,  CD11c-T-bet- B cells from Bm12-induced lupus T-bet reporter mice</name><description>To test the chromatin accessibility of different immune cell subsets, we isolated naive B cells CD11c+T-bet+ B cells,  CD11c-T-bet- B cells by flow cytometry from Bm12-induced lupus T-bet reporter mice and performed ATAC assay.</description><dates><release>2025-05-16T00:00:00Z</release><modification>2023-05-16T15:29:45.616Z</modification><creation>2023-05-16T15:29:45.616Z</creation></dates><accession>E-MTAB-12903</accession><cross_references><ENA>ERP147273</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0007045</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>