<HashMap><database>biostudies-arrayexpress</database><scores/><additional><omics_type>Metabolomics</omics_type><omics_type>Unknown</omics_type><omics_type>Transcriptomics</omics_type><omics_type>Genomics</omics_type><omics_type>Proteomics</omics_type><submitter>Charles Girardot</submitter><instrument_platform>NextSeq 500</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-13692</full_dataset_link><description>To describe chromatin accessibility changes associated with differentiation of mouse presomitic mesoderm (PSM) cells into somites, ATAC sequencing (paired-end) was performed using non-cultured, wild-type PSM tissues that were microdissected into tailbud, posterior PSM, anterior PSM, and somite regions. Omni-ATAC protocol was used, and each condition includes six biological replicates.�</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - paired-end sequencing on illumina NextSeq 500</sample_protocol><sample_protocol>Library Construction - ATAC-seq library were prepared following the Omni-ATAC protocol (Corces et al., Nat Methods, 2017).</sample_protocol><sample_protocol>Growth Protocol - Mice were crossed, and females were dissected 10 days after a detection of vaginal plug, and the PSM tissues isolated.</sample_protocol><sample_protocol>Growth Protocol - PSM explants of E10.5 wild-type embryos were microdissected into tail bud, posterior PSM, anterior PSM, and somite regions by micro scalpel in cold PBS. Each tissue region was transferred into a micro well (ibidi, #80486) and mechanically dissociated to a cell suspension in 4.2 �l cold PBS. Finally, 0.7 �l and 3.3 �l cell suspensions were used for RNA-sequencing (RNA-seq) and ATAC-sequencing (ATAC-seq), respectively</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>Charles Girardot</pubmed_authors><pubmed_authors>Emilia Esposito</pubmed_authors></additional><is_claimable>false</is_claimable><name>ATAC-seq of wild-type mouse PSM tissues that were microdissected into tailbud, posterior PSM, anterior PSM, and somite regions</name><description>To describe chromatin accessibility changes associated with differentiation of mouse presomitic mesoderm (PSM) cells into somites, ATAC sequencing (paired-end) was performed using non-cultured, wild-type PSM tissues that were microdissected into tailbud, posterior PSM, anterior PSM, and somite regions. Omni-ATAC protocol was used, and each condition includes six biological replicates.�</description><dates><release>2025-08-06T00:00:00Z</release><modification>2025-08-07T00:01:25.679Z</modification><creation>2024-01-04T14:11:51.262Z</creation></dates><accession>E-MTAB-13692</accession><cross_references><ENA>ERP156459</ENA><EFO>EFO_0007045</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>