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    <IDENTIFIERS>
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      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35778_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP129226">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP129226</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB45097</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA8654756 for study accession PRJEB45097.  This is part of an Illumina multiplexed sequencing run (35778_2). This submission includes reads tagged with the sequence GGGAGCTG. Library was made using a Hi-C - Arima v2 kit with restriction enzyme motif ^GATC,G^ANTC,C^TNAG,T^TAA.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>ERS6339307</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA8654756</EXTERNAL_ID>
        </IDENTIFIERS>
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        <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>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX6465916</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35787_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP129226">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP129226</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB45097</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA8654750 for study accession PRJEB45097.  This is part of an Illumina multiplexed sequencing run (35787_7). This submission includes reads tagged with the sequence ACACTGTT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS6339301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA8654750</EXTERNAL_ID>
        </IDENTIFIERS>
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        <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>ERX6465917</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35787_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP129226">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP129226</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB45097</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA8654750 for study accession PRJEB45097.  This is part of an Illumina multiplexed sequencing run (35787_7). This submission includes reads tagged with the sequence CAGGATGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS6339301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS6339301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA8654750</EXTERNAL_ID>
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        <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>ERX6465918</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35787_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP129226">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP129226</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB45097</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA8654750 for study accession PRJEB45097.  This is part of an Illumina multiplexed sequencing run (35787_7). This submission includes reads tagged with the sequence GGCTGAAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS6339301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS6339301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA8654750</EXTERNAL_ID>
        </IDENTIFIERS>
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        <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>ERX6465919</PRIMARY_ID>
      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_35787_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>HiSeq X Ten paired end sequencing</TITLE>
    <STUDY_REF accession="ERP129226">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP129226</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB45097</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA8654750 for study accession PRJEB45097.  This is part of an Illumina multiplexed sequencing run (35787_7). This submission includes reads tagged with the sequence TTTACCCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS6339301">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS6339301</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA8654750</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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