<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087220">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087220</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087221">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087221</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087222">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087222</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087223">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087223</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087224">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087224</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087225">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087225</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087226">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087226</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087227">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087227</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087228">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087228</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087229">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087229</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087230">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087230</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087231">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087231</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087232">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087232</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087233">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087233</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087234">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087234</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087235">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087235</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087236">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087236</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087237">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087237</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087238">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087238</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087239">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087239</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087240">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087240</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087241">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087241</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087242">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087242</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087243">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087243</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087244">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087244</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087245">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087245</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087246">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087246</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087247">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087247</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087248">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087248</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_1#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087249">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087249</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087250">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087250</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087251">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087251</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087252">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087252</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087253">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087253</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087254">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087254</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087255">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087255</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087256">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087256</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087257">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087257</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087258">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087258</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087259">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087259</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087260">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087260</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087261">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087261</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087262">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087262</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087263">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087263</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087264">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087264</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087265">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087265</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087266">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087266</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087267">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087267</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087268">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087268</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087269">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087269</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087270">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087270</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087271">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087271</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087272">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087272</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087273">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087273</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087274">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087274</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087275">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087275</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087276">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087276</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087277">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087277</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087278">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087278</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_2#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087279">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087279</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_2).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087280">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087280</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087281">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087281</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087282">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087282</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087283">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087283</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087284">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087284</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087285">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087285</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087286">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087286</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087287">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087287</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087288">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087288</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087289">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087289</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087290">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087290</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087291">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087291</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087292">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087292</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087293">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087293</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087294">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087294</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087295">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087295</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087296">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087296</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087297">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087297</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087298">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087298</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087299">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087299</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087300">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087300</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087301">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087301</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087302">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087302</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087303">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087303</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087304">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087304</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087305">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087305</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087306">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087306</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087307">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087307</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087308">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087308</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_3#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087309">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087309</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_3#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_3#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_3).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087310">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087310</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087311">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087311</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087312">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087312</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087313">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087313</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087314">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087314</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087315">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087315</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087316">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087316</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087317">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087317</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087318">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087318</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087319">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087319</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087320">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087320</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087321">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087321</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087322">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087322</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#14" accession="ERX1087323">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087323</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087324">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087324</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087325">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087325</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087326">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087326</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087327">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087327</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087328">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087328</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087329">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087329</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087330">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087330</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087331">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087331</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087332">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087332</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087333">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087333</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087334">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087334</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087335">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087335</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087336">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087336</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087337">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087337</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087338">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087338</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_4#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087339">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087339</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_4#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_4#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_4).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087340">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087340</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087341">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087341</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087342">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087342</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087343">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087343</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_5#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_5#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_5#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_5).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087385">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087386">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087387">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087388">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087389">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087390">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087391">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087392">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087393">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087394">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087395">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087396">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_6#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_6#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_6#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_6).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087416">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087417">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087418">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087419">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087420">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087421">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087422">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087423">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087424">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087425">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087426">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087427">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087428">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_7#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087429">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_7#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_7#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_7).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087430">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241974, constructed from sample accession ERS758334 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758334" refname="HT29C3_1-sc-2318403" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758334</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462653</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_1-sc-2318403</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087431">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241975, constructed from sample accession ERS758335 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence CGATGTTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758335" refname="HT29C3_2-sc-2318404" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758335</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462654</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_2-sc-2318404</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087432">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241976, constructed from sample accession ERS758336 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758336" refname="HT29C3_3-sc-2318405" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758336</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462655</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_3-sc-2318405</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087433">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241977, constructed from sample accession ERS758337 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758337" refname="HT29C3_4-sc-2318406" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758337</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462656</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_4-sc-2318406</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087434">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241978, constructed from sample accession ERS758338 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758338" refname="HT29C3_5-sc-2318407" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758338</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462657</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_5-sc-2318407</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087435">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241979, constructed from sample accession ERS758339 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758339" refname="HT29C3_6-sc-2318408" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758339</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462658</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_6-sc-2318408</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087436">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241980, constructed from sample accession ERS758340 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758340" refname="HT29C3_7-sc-2318409" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758340</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462659</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_7-sc-2318409</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087437">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241981, constructed from sample accession ERS758341 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758341" refname="HT29C3_8-sc-2318410" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758341</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462660</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_8-sc-2318410</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087438">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241982, constructed from sample accession ERS758342 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758342" refname="HT29C3_9-sc-2318411" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758342</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462661</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_9-sc-2318411</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087439">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241983, constructed from sample accession ERS758343 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758343" refname="HT29C3_10-sc-2318412" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758343</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462662</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_10-sc-2318412</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087440">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241984, constructed from sample accession ERS758344 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758344" refname="HT29C3_11-sc-2318413" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758344</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462663</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_11-sc-2318413</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087441">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241985, constructed from sample accession ERS758345 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758345" refname="HT29C3_12-sc-2318414" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758345</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462664</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_12-sc-2318414</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087442">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241986, constructed from sample accession ERS758346 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758346" refname="HT29C3_13-sc-2318415" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758346</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462665</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_13-sc-2318415</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087443">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241987, constructed from sample accession ERS758347 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758347" refname="HT29C3_14-sc-2318416" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758347</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462666</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_14-sc-2318416</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087444">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241988, constructed from sample accession ERS758348 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758348" refname="HT29C3_15-sc-2318417" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758348</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462667</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_15-sc-2318417</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087445">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241989, constructed from sample accession ERS758349 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758349" refname="HT29C3_16-sc-2318418" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758349</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462668</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_16-sc-2318418</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087446">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241990, constructed from sample accession ERS758350 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758350" refname="HT29C3_17-sc-2318419" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758350</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462669</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_17-sc-2318419</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087447">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241991, constructed from sample accession ERS758351 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758351" refname="HT29C3_18-sc-2318420" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758351</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462670</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_18-sc-2318420</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087448">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241992, constructed from sample accession ERS758352 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758352" refname="HT29C3_19-sc-2318421" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758352</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462671</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_19-sc-2318421</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087449">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241993, constructed from sample accession ERS758353 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758353" refname="HT29C3_20-sc-2318422" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758353</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462672</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_20-sc-2318422</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087450">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241994, constructed from sample accession ERS758354 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758354" refname="HT29C3_21-sc-2318423" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758354</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462673</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_21-sc-2318423</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087451">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241995, constructed from sample accession ERS758355 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758355" refname="HT29C3_22-sc-2318424" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758355</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462674</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_22-sc-2318424</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087452">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241996, constructed from sample accession ERS758356 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758356" refname="HT29C3_23-sc-2318425" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758356</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462675</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_23-sc-2318425</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087453">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241997, constructed from sample accession ERS758357 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758357" refname="HT29C3_24-sc-2318426" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758357</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462676</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_24-sc-2318426</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087454">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241998, constructed from sample accession ERS758358 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758358" refname="HT29C3_25-sc-2318427" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758358</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462677</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_25-sc-2318427</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087455">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14241999, constructed from sample accession ERS758359 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758359" refname="HT29C3_26-sc-2318428" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758359</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462678</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_26-sc-2318428</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14241999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087456">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242000, constructed from sample accession ERS758360 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758360" refname="HT29C3_27-sc-2318429" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758360</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462679</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_27-sc-2318429</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087457">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242001, constructed from sample accession ERS758361 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758361" refname="HT29C3_28-sc-2318430" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758361</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462680</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_28-sc-2318430</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087458">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242002, constructed from sample accession ERS758362 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758362" refname="HT29C3_29-sc-2318431" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758362</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462681</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_29-sc-2318431</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" alias="SC_EXP_16807_8#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1087459">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1087459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16807_8#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16807_8#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing</TITLE>
    <STUDY_REF accession="ERP005600" refname="CRISPR_gRNA_library_validation-sc-3081" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP005600</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">CRISPR_gRNA_library_validation-sc-3081</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 14242003, constructed from sample accession ERS758363 for study accession ERP005600.  This is part of an Illumina multiplexed sequencing run (16807_8).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS758363" refname="HT29C3_30-sc-2318432" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS758363</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3462682</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">HT29C3_30-sc-2318432</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>14242003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
