<HashMap><database>biostudies-arrayexpress</database><scores/><additional><submitter>Stijn Verwaerde</submitter><organism>Mus musculus</organism><software>bowtie2</software><software>DiffBind</software><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/E-MTAB-16047</full_dataset_link><description>CUT&amp;RUN of IRF4 in murine alveolar macrophages after 3 I.T. doses of PBS (control) or IL-33 treatment.</description><repository>biostudies-arrayexpress</repository><sample_protocol>Library Construction - Libraries were prepared using the NEBNext Ultra II DNA Library Prep Kit for Illumina according to the manufacturer’s instructions. Cleanup of libraries was performed with AMPure XP beads (Beckman Coulter).</sample_protocol><sample_protocol>Sequencing - Libraries were sequenced on NovaSeq 6000 (Illumina) to generate paired 50-bp reads.</sample_protocol><sample_protocol>Nucleic Acid Extraction - CUT and RUN was carried out with minor adaptations from the protocol  described in the following reference:  \"Skene, P. J., Henikoff, J. G. &amp; Henikoff, S. Targeted in situ genome-wide profiling with high efficiency for low cell numbers. Nat Protoc 13, 1006–1019 (2018)..\"  Additional information can be found in original publication.</sample_protocol><sample_protocol>Sample Collection - Alveolar macrophages were collected by bronchoalveolar lavage (BAL). BAL was lightly fixed with formaldehyde (final concentration of 0.1%) quenched with glycine and single-cell suspension was stained with monoclonal antibodies followed by cell sorting. 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 carry-over of E. coli DNA from purification of pA/MNase. Normalization step a was performed with the DiffBind package.</data_protocol><data_protocol>Sequence Alignment - Mapping was performed to a mouse reference genome (mm39) with bowtie2 (v2.5.3). The bam files were ordered and filtered to contain fragments with lenght ≤150 bp. The filtered and sorted bam files were used for further analysis. For normalization purpose, bam files with the sequences mapped to E.coli reference genome (eschColi_K12) were also generated.</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>CUT&amp;RUN</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>IRF4 CUT&amp;RUN sequencing of murine alveolar macrophages after IL-33 treatment</name><description>CUT&amp;RUN of IRF4 in 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>2026-04-17T17:06:39.702Z</modification><creation>2025-11-13T14:14:29.116Z</creation></dates><accession>E-MTAB-16047</accession><cross_references><ENA>ERP184014</ENA><EFO>EFO_0002944</EFO><EFO>EFO_0009973</EFO><EFO>EFO_0004170</EFO><EFO>EFO_0004917</EFO><EFO>EFO_0005518</EFO><EFO>EFO_0003816</EFO><EFO>EFO_0004184</EFO></cross_references></HashMap>