<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE106730" accession="SRP124726">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP124726</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA417817</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE106730</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Divergent principles specifying inflammatory versus antiviral transcriptional programs in dendritic cells [ChIP-seq]</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Stimulus-specific gene expression programs are enabled by enhancers, on which stimulus-regulated transcription factors (SRTFs) can land in a cell type- and stimulus-dependent manner. In this study, we identified the key features of enhancers that mediate differential responses to Toll-like receptor (TLR)-stimulation. We characterized the TLR3- and TLR9-induced programs and enhancers in CD8+ dendritic cells.The relevance of these features has been confirmed via machine learning application and by mapping SRTF-binding. Overall design: CD8-positive dendritic cells were left unstimulated or were treated for the indicated periods of time (6h or 90 mins) with 5 mg/ml of high molecular weight Polyinosinic-polycytidylic acid (pIC) or 1 mM class B CpG oligonucleotide 1826 (CpG).</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE106730</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>parent_bioproject</TAG>
        <VALUE>PRJNA417853</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
