<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2975737" accession="SRX3638881">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638881</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975737: U937 cell line DMSO treated rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905130">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905130</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975737</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975737</ID>
          <LABEL>GSM2975737</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975737</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2975738" accession="SRX3638882">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638882</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975738: U937 cell line DMSO treated rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905132">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905132</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975738</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975738</ID>
          <LABEL>GSM2975738</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975738</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2975739" accession="SRX3638883">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638883</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975739: U937 cell line DMSO treated rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905131">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905131</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975739</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975739</ID>
          <LABEL>GSM2975739</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975739</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2975740" accession="SRX3638884">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638884</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975740: U937 cell line BRD3731 treated rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905133">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905133</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975740</ID>
          <LABEL>GSM2975740</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975740</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2975741" accession="SRX3638885">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638885</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975741</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975741: U937 cell line BRD3731 treated rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905134">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905134</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975741</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975741</ID>
          <LABEL>GSM2975741</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975741</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2975742" accession="SRX3638886">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3638886</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2975742</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2975742: U937 cell line BRD3731 treated rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP131964" refname="GSE109986">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP131964</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2905135">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2905135</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2975742</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from cells with the RNeasy Kit and on-column DNA digestion (Qiagen). RNA libraries were prepared for sequencing using standard Illumina 1.9 protocols Strand-specific mRNA seq libraries were pooled and sequenced on a NextSeq500 instrument with single-end 75bp reads to a depth of 20-30 M reads/sample at the Molecular Biology Core Facilities (Dana-Farber Cancer Institute, Boston, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302975742</ID>
          <LABEL>GSM2975742</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2975742</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
