<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="ERX6313494" alias="SC_EXP_36148_3#41" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX6313494</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_36148_3#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP131581">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP131581</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB47303</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7521999 for study accession PRJEB47303.  This is part of an Illumina multiplexed sequencing run (36148_3). This submission includes reads tagged with the sequence CCTCATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5278478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5278478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7521999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium genome</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX6313495" alias="SC_EXP_36148_3#42" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX6313495</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_36148_3#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP131581">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP131581</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB47303</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7521999 for study accession PRJEB47303.  This is part of an Illumina multiplexed sequencing run (36148_3). This submission includes reads tagged with the sequence AGCATCCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5278478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5278478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7521999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium genome</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX6313496" alias="SC_EXP_36148_3#43" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX6313496</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_36148_3#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP131581">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP131581</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB47303</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7521999 for study accession PRJEB47303.  This is part of an Illumina multiplexed sequencing run (36148_3). This submission includes reads tagged with the sequence GTGGCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5278478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5278478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7521999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium genome</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX6313497" alias="SC_EXP_36148_3#44" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX6313497</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_36148_3#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP131581">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP131581</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB47303</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7521999 for study accession PRJEB47303.  This is part of an Illumina multiplexed sequencing run (36148_3). This submission includes reads tagged with the sequence TAATGGGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5278478">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5278478</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7521999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium genome</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX6313498" alias="SC_EXP_39723_8#7" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX6313498</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_39723_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 4000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP131581">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP131581</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB47303</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7521997 for study accession PRJEB47303.  This is part of an Illumina multiplexed sequencing run (39723_8). This submission includes reads tagged with the sequence CTGATGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5278476">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5278476</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7521997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PolyA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="200"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA PolyA</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
