<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2157513" accession="SRX1771654">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1771654</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2157513</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2157513: UT-R1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP075351" refname="GSE81575">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP075351</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1443723">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1443723</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2157513</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>Cancer cells were lysed on culture dishes and RNA was extracted using TOTLA RNA I etraction kit (Omega-Biotek). Total RNA was treated with DNase (ThermoFisher RapidOut) prior to library preparation. Directional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302157513</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2157513</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2157514" accession="SRX1771655">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1771655</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2157514</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2157514: UT-R2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP075351" refname="GSE81575">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP075351</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1443724">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1443724</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2157514</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>Cancer cells were lysed on culture dishes and RNA was extracted using TOTLA RNA I etraction kit (Omega-Biotek). Total RNA was treated with DNase (ThermoFisher RapidOut) prior to library preparation. Directional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302157514</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2157514</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2157515" accession="SRX1771656">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1771656</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2157515</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2157515: AB-C1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP075351" refname="GSE81575">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP075351</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1443726">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1443726</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2157515</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>Cancer cells were lysed on culture dishes and RNA was extracted using TOTLA RNA I etraction kit (Omega-Biotek). Total RNA was treated with DNase (ThermoFisher RapidOut) prior to library preparation. Directional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302157515</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2157515</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2157516" accession="SRX1771657">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1771657</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2157516</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2157516: AB-C2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP075351" refname="GSE81575">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP075351</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1443725">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1443725</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2157516</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>Cancer cells were lysed on culture dishes and RNA was extracted using TOTLA RNA I etraction kit (Omega-Biotek). Total RNA was treated with DNase (ThermoFisher RapidOut) prior to library preparation. Directional RNA-seq libraries were prepared from 500ng total RNA using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302157516</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2157516</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
