<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_14624_3#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX681994">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681994</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961842, constructed from sample accession ERS555177 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555177" refname="sample_1-sc-2134900" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785455</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_1-sc-2134900</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961842</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_3#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX681995">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681995</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961843, constructed from sample accession ERS555178 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555178" refname="sample_2-sc-2134901" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785456</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_2-sc-2134901</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961843</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_3#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX681996">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681996</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961844, constructed from sample accession ERS555179 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555179" refname="sample_3-sc-2134902" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555179</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785457</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_3-sc-2134902</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961844</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_3#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX681997">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681997</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961845, constructed from sample accession ERS555180 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555180" refname="sample_4-sc-2134903" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555180</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785458</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_4-sc-2134903</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961845</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_3#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX681998">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681998</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961846, constructed from sample accession ERS555181 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555181" refname="sample_5-sc-2134904" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555181</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785459</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_5-sc-2134904</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961846</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_3#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX681999">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX681999</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_3#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_3#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961847, constructed from sample accession ERS555182 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_3).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555182" refname="sample_6-sc-2134905" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555182</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785460</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_6-sc-2134905</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961847</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="479" NOMINAL_SDEV="133"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX682000">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682000</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961848, constructed from sample accession ERS555183 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TAACGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555183" refname="sample_7-sc-2134906" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555183</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785461</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_7-sc-2134906</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961848</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX682001">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682001</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961849, constructed from sample accession ERS555184 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TTGGTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555184" refname="sample_8-sc-2134907" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555184</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785462</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_8-sc-2134907</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961849</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX682002">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682002</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961850, constructed from sample accession ERS555185 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TGAACTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555185" refname="sample_9-sc-2134908" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555185</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785463</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_9-sc-2134908</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961850</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX682003">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682003</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961851, constructed from sample accession ERS555186 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TACTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555186" refname="sample_10-sc-2134909" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555186</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785464</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_10-sc-2134909</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961851</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX682004">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682004</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961852, constructed from sample accession ERS555187 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TCTCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555187" refname="sample_11-sc-2134910" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555187</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785465</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_11-sc-2134910</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961852</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14624_4#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX682005">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX682005</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14624_4#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14624_4#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007103" refname="Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007103</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Genome_sequencing_of_virus_associated_B_cell_lymphomas-sc-3320</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11961853, constructed from sample accession ERS555188 for study accession ERP007103.  This is part of an Illumina multiplexed sequencing run (14624_4).  This submission includes reads tagged with the sequence TCAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS555188" refname="sample_12-sc-2134911" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS555188</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2785466</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">sample_12-sc-2134911</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11961853</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="497" NOMINAL_SDEV="137"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Standard</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
