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    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917330</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35436_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7522766 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (35436_6). This submission includes reads tagged with the sequence ACATTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5279244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5279244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7522766</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917334</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_46781_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA12219723 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (46781_2). This submission includes reads tagged with the sequence CTTTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9816706">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9816706</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12219723</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
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        <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 NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917331</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35436_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7522766 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (35436_6). This submission includes reads tagged with the sequence TTTGGGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5279244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5279244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7522766</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917329</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35430_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7522765 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (35430_4). This submission includes reads tagged with the sequence GACGCTAA. Library was made using a Hi-C - Arima v2 kit with restriction enzyme motif ^GATC,G^ANTC,C^TNAG,T^TAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5279243">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5279243</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7522765</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Hi-C</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hi-C - Arima v2</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917332</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35436_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7522766 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (35436_6). This submission includes reads tagged with the sequence CAGCCCAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5279244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5279244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7522766</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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11917335" alias="SC_EXP_47798_1#3" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917335</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_47798_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA12219722 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (47798_1). This submission includes reads tagged with the sequence GTACCAAA. Library was made using a Hi-C - Arima v2 kit with restriction enzyme motif ^GATC,G^ANTC,C^TNAG,T^TAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS9816705">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS9816705</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA12219722</EXTERNAL_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>Hi-C</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Restriction Digest</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Hi-C - Arima v2</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX11917333" alias="SC_EXP_35436_6#8" center_name="WELLCOME SANGER INSTITUTE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX11917333</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35436_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP156895">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP156895</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB72110</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7522766 for study accession PRJEB72110.  This is part of an Illumina multiplexed sequencing run (35436_6). This submission includes reads tagged with the sequence GGCAATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS5279244">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS5279244</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7522766</EXTERNAL_ID>
        </IDENTIFIERS>
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      <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>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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