<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX22253813" alias="GSM7868428_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22253813</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7868428_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7868428: RCC4, IFNg + TNF treated, biol rep 3, Illumina; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP468887">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468887</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1032888</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19307048">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19307048</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7868428</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7868428</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>Cells were first washed with ice-cold PBS (Gibco), followed by lysis with Qiazol (Qiagen). Total RNA was extracted using RNeasy RNA extraction kit (Qiagen) with an additional Dnase I digestion (QIAGEN) according to manufacturer's instruction. Poly(A)+ RNA molecules were enriched from total RNA with the Dynabeads mRNA purification kit (Thermo Fisher). Sequencing libraries were generated using Ultra III directional RNA library prep kit (NEB) according to manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22253814" alias="GSM7868426_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22253814</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7868426_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7868426: RCC4, IFNg + TNF treated, biol rep 1, Illumina; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP468887">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468887</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1032888</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19307049">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19307049</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7868426</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7868426</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>Cells were first washed with ice-cold PBS (Gibco), followed by lysis with Qiazol (Qiagen). Total RNA was extracted using RNeasy RNA extraction kit (Qiagen) with an additional Dnase I digestion (QIAGEN) according to manufacturer's instruction. Poly(A)+ RNA molecules were enriched from total RNA with the Dynabeads mRNA purification kit (Thermo Fisher). Sequencing libraries were generated using Ultra III directional RNA library prep kit (NEB) according to manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX22253815" alias="GSM7868427_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX22253815</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM7868427_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM7868427: RCC4, IFNg + TNF treated, biol rep 2, Illumina; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP468887">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP468887</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA1032888</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS19307050">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19307050</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM7868427</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM7868427</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>Cells were first washed with ice-cold PBS (Gibco), followed by lysis with Qiazol (Qiagen). Total RNA was extracted using RNeasy RNA extraction kit (Qiagen) with an additional Dnase I digestion (QIAGEN) according to manufacturer's instruction. Poly(A)+ RNA molecules were enriched from total RNA with the Dynabeads mRNA purification kit (Thermo Fisher). Sequencing libraries were generated using Ultra III directional RNA library prep kit (NEB) according to manufacturer's instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 3000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
