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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4395159" alias="3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4395159</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4301351">3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq for variant calling performance, independent sample</TITLE>
    <STUDY_REF accession="SRP153933">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP153933</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4301351">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>M0253 by mixing Horizon Dxs Tru-Q 7 reference standard (verified 1.3%-tier variants) with Tru-Q 0 231 (wild-type) at 1:1 ratio. The Horizon sample was sequenced using QIAseq Human Actionable Solid Tumor 232 Panel (catalog number DHS-101Z)</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3550342">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3550342</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|rp2801">M0253</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4395160" alias="1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4395160</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4301351">1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq for 0.5% variant calling performance</TITLE>
    <STUDY_REF accession="SRP153933">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP153933</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4301351">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>N13532 was generated by adding 1% mixture of NA12878 to NA24385 and sequenced using QIASeq DNA catalog ID : CDHS-13532Z-10181</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3550343">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3550343</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|rp2801">N13532</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4395161" alias="2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4395161</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4301351">2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>DNA-Seq for 0.5% variant calling performance , enriched for INDELS</TITLE>
    <STUDY_REF accession="SRP153933">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP153933</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4301351">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>N0261 was generated by adding 1% mixture of NA12878 to NA24385 and sequenced using QIAseq DNA catalog ID :   CDHS-13907Z-562</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3550344">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3550344</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|rp2801">N0261</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
