<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX20314456" alias="GSM7331471_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314456</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331471_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331471: YRG cells, control, untreated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638865">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638865</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331471</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314457" alias="GSM7331472_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314457</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331472_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331472: YRG cells, SETDB1-sg1, untreated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638866">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638866</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331472</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314458" alias="GSM7331473_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314458</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331473_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331473: YRG cells, SETDB1-sg2, untreated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638869">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638869</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331473</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314459" alias="GSM7331474_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314459</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331474_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331474: YRG cells, control, PBS treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638867">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638867</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331474</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314460" alias="GSM7331475_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314460</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331475_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331475: YRG cells, control, aIFNAR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638868">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638868</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331475</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314461" alias="GSM7331476_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314461</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331476_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331476: YRG cells, control, aIFNGR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638870">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638870</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331476</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314462" alias="GSM7331478_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314462</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331478_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331478: YRG cells, SETDB1-sg1, PBS treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638871">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638871</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331478</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314463" alias="GSM7331479_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314463</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331479_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331479: YRG cells, SETDB1-sg1, aIFNAR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638872">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638872</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331479</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314464" alias="GSM7331480_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314464</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331480_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331480: YRG cells, SETDB-sg1, aIFNGR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638873">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638873</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331480</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314465" alias="GSM7331481_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314465</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331481_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331481: YRG cells, SETDB1-sg2, PBS treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638874">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638874</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331481</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314466" alias="GSM7331482_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314466</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331482_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331482: YRG cells, SETDB1-sg2, aIFNAR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638876">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638876</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331482</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX20314467" alias="GSM7331483_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX20314467</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7331483_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7331483: YRG cells, SETDB-sg2, aIFNGR treated; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP437493">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP437493</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA971946</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS17638875">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS17638875</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7331483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7331483</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>1x106 cells were pelleted, and RNA isolated using RNeasy kit, supplemented with QIAshredder and DNase treatment (Qiagen). TruSeq stranded library preparation was performed by the YCGA according to manufacturer protocol.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
