<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Stijn Verwaerde</submitter><organism>Mus musculus</organism><software>ChromatinHD</software><software>bowtie2</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16048</full_dataset_link><description>ATAC-sequencing of murine alveolar macrophages after 3 I.T. doses of PBS (control) or IL-33 treatment.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Sequencing - Libraries were sequenced on NovaSeq 6000 (Illumina) to generate paired 50-bp reads.</sample_protocol><sample_protocol>Library Construction - Transposed DNA was amplified using a NEBNext High Fidelity 2× PCR Master Mix (New England Biolabs) with indexed primers. Libraries were purified using SPRIselect beads (Beckman Coulter) to remove primer dimers.</sample_protocol><sample_protocol>Sample Collection - Alveolar macrophages were collected by bronchoalveolar lavage (BAL). Single-cell suspension was stained with monoclonal antibodies followed by cell sorting. Additional information can be found in original publication.</sample_protocol><sample_protocol>Nucleic Acid Extraction - ATAC-seq was carried out with minor adaptations from the protocol  described in the following reference:  \"Buenrostro, J. D., Wu, B., Chang, H. Y. &amp; Greenleaf, W. J. ATAC-seq: A method for assaying chromatin accessibility genome-wide. Curr Protoc Mol Biol 2015, 21.29.1-21.29.9 (2015).\"  Additional information can be found in original publication.</sample_protocol><figure_sub>Organization</figure_sub><figure_sub>MINSEQE Score</figure_sub><figure_sub>Assays and Data</figure_sub><figure_sub>Processed Data</figure_sub><figure_sub>MAGE-TAB Files</figure_sub><data_protocol>Data Transformation - Data were normalized based on library size and further analysis was performed  using ChromatinHD.</data_protocol><data_protocol>Sequence Alignment - Mapping was performed to a mouse reference genome (mm39) with bowtie2 (v2.5.3). Duplicated reads and non-aligned reads were removed from the final bam files.</data_protocol><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><instrument_platform>Illumina NovaSeq 6000</instrument_platform><study_type>ATAC-seq</study_type><species>Mus musculus</species><pubmed_title>Type-2 Innate Lymphocytes Trigger an Inflammatory Switch in Alveolar Macrophages</pubmed_title><pubmed_authors>Stijn Verwaerde</pubmed_authors><pubmed_authors>Jean-François Hastir</pubmed_authors><pubmed_authors>Stijn Verwaerde, Jean-François Hastir, Sjoerd Schetters, Ursula Smole, Leen Seys,  Antonio P. Baptista, Kieran English, Martijn J. Schuijs, Helena Aegerter, Karel FA Van Damme, Aimée Bugler-Lamb, Nikita Gerebtsov, Wendy Toussaint, Tatsuma Ban, Tomohiko Tamura,  Florent Ginhoux, Zhaoyuan Liu, Wouter Saelens, Hamida Hammad, Martin Guilliams, Bart N. Lambrecht1, 2,8</pubmed_authors></additional><is_claimable>false</is_claimable><name>ATAC-sequencing of murine alveolar macrophages after IL-33 treatment</name><description>ATAC-sequencing of murine alveolar macrophages after 3 I.T. doses of PBS (control) or IL-33 treatment.</description><dates><release>2025-12-12T00:00:00Z</release><modification>2026-05-27T12:48:33.534Z</modification><creation>2025-11-13T14:20:35.27Z</creation></dates><accession>E-MTAB-16048</accession><cross_references><ENA>ERP184015</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0007045</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>