<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17426742" alias="Sample_Fo5-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426742</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982218">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982218</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426743" alias="Sample_Fo5-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426743</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982219">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982219</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426744" alias="Sample_Fo5-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426744</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982220">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982220</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426745" alias="Sample_Fo5-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426745</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982221">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982221</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426746" alias="Sample_Fo5-5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426746</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982222">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982222</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426747" alias="Sample_Fo5-Tuc-01">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426747</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-Tuc-01</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982223">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982223</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-Tuc-01</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-Tuc-01</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426748" alias="Sample_Fo5-Tuc-02">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426748</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-Tuc-02</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982224">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982224</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-Tuc-02</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-Tuc-02</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426749" alias="Sample_Fo5-Tuc-03">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426749</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-Tuc-03</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982225">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982225</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-Tuc-03</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-Tuc-03</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17426750" alias="Sample_Fo5-Tuc-04">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17426750</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB12013945">Sample_Fo5-Tuc-04</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of mus musculus: adult female breast</TITLE>
    <STUDY_REF accession="SRP395636">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395636</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB12013945">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>RNA was extracted from Fo5 tumors treated in vivo with tucatinib 50 mg/kg or vehicle (methyl cellulose 0.5%) for 10 days using TRIzol Reagent with the PureLink RNA Mini Kit (Invitrogen, Thermo Fisher Scientific, Waltham, MA, USA). Quantity and integrity of the total RNA was checked using a TapeStation 2200 (Agilent Technologies) and 500 ng used for library preparation according to standard protocols (NEBNext Ultra II Directional RNA Library Prep Kit for Illumina and NEBNext Poly(A) mRNA Magnetic Isolation Module, NEB). Indexed libraries were pooled and sequenced on a NextSeq500 flowcell (Illumina) to generate 25-50 million paired-end 75 bp reads per sample.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS14982226">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14982226</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|franco.caramia@petermac.org">Sample_Fo5-Tuc-04</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Sample_Fo5-Tuc-04</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
