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      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_36957_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7746847 for study accession PRJEB48586.  This is part of an Illumina multiplexed sequencing run (36957_3). This submission includes reads tagged with the sequence GCACTTGC. 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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        <LIBRARY_LAYOUT>
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        </LIBRARY_LAYOUT>
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      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_37177_4#45</SUBMITTER_ID>
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    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
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      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7746848 for study accession PRJEB48586.  This is part of an Illumina multiplexed sequencing run (37177_4). This submission includes reads tagged with the sequence GCACAATG.</DESIGN_DESCRIPTION>
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    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7746848 for study accession PRJEB48586.  This is part of an Illumina multiplexed sequencing run (37177_4). This submission includes reads tagged with the sequence CTTGGTAC.</DESIGN_DESCRIPTION>
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    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7746848 for study accession PRJEB48586.  This is part of an Illumina multiplexed sequencing run (37177_4). This submission includes reads tagged with the sequence TGCACCGT.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS5494195</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA7746848</EXTERNAL_ID>
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      <SUBMITTER_ID namespace="WELLCOME SANGER INSTITUTE">SC_EXP_37177_4#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina NovaSeq 6000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP132974">
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        <PRIMARY_ID>ERP132974</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJEB48586</EXTERNAL_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of sample accession SAMEA7746848 for study accession PRJEB48586.  This is part of an Illumina multiplexed sequencing run (37177_4). This submission includes reads tagged with the sequence AAGTTGCA.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>ERS5494195</PRIMARY_ID>
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        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Chromium genome</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
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