<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM5111608" accession="SRX10176118">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176118</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111608</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111608: Hepatocyte WT rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325132">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325132</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111608</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111608</ID>
          <LABEL>GSM5111608</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111608</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111609" accession="SRX10176119">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176119</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111609</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111609: Hepatocyte WT rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325133">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325133</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111609</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111609</ID>
          <LABEL>GSM5111609</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111609</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111610" accession="SRX10176120">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176120</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111610</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111610: Hepatocyte LSKO rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325134">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325134</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111610</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111610</ID>
          <LABEL>GSM5111610</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111610</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111611" accession="SRX10176121">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176121</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111611</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111611: Hepatocyte LSKO rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325135">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325135</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111611</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111611</ID>
          <LABEL>GSM5111611</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111611</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111612" accession="SRX10176122">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176122</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111612</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111612: Hepatocyte LSKO Mn; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325136">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325136</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111612</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111612</ID>
          <LABEL>GSM5111612</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111612</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111613" accession="SRX10176123">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176123</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111613</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111613: Hepatocyte LSKO Fe; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325137">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325137</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111613</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111613</ID>
          <LABEL>GSM5111613</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111613</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111614" accession="SRX10176124">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176124</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111614</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111614: Hepatocyte LSKO Se; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325138">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325138</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111614</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111614</ID>
          <LABEL>GSM5111614</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111614</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM5111615" accession="SRX10176125">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX10176125</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM5111615</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM5111615: Hepatocyte LSKO Zn; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP308366" refname="GSE167626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP308366</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS8325139">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS8325139</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5111615</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed in Trizol reagent and transferred to RNAse free tubes for processing. Using the Qiagen RNeasy Mini Kit (#74104), RNA was extracted and then cleaned using the Monarch RNA Cleanup Kit (#T2050S) from New England BioLabs. Total RNA was quantified and sent to GENEWIZ for library construction. RNA libraries were prepared for sequencing using standard Illumina protocols at GENEWIZ</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>305111615</ID>
          <LABEL>GSM5111615</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM5111615</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
