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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_14262_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX662548">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662548</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904945, constructed from sample accession ERS554170 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence ATGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554170" refname="ZMP_phenotype_114_1_RNASeq_3-sc-2133720" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784426</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_3-sc-2133720</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904945</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX662549">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662549</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904946, constructed from sample accession ERS554171 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence CCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554171" refname="ZMP_phenotype_114_1_RNASeq_4-sc-2133721" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784427</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_4-sc-2133721</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX662550">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662550</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904947, constructed from sample accession ERS554172 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554172" refname="ZMP_phenotype_114_1_RNASeq_5-sc-2133722" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784428</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_5-sc-2133722</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX662551">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662551</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904948, constructed from sample accession ERS554173 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554173" refname="ZMP_phenotype_114_1_RNASeq_6-sc-2133723" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784429</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_6-sc-2133723</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX662552">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662552</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904949, constructed from sample accession ERS554174 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GTGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554174" refname="ZMP_phenotype_114_1_RNASeq_7-sc-2133724" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784430</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_7-sc-2133724</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX662553">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662553</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904950, constructed from sample accession ERS554175 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554175" refname="ZMP_phenotype_114_1_RNASeq_8-sc-2133725" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784431</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_8-sc-2133725</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX662554">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662554</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904951, constructed from sample accession ERS554176 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence CGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554176" refname="ZMP_phenotype_114_1_RNASeq_9-sc-2133726" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784432</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_9-sc-2133726</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904951</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX662555">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662555</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904952, constructed from sample accession ERS554177 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554177" refname="ZMP_phenotype_114_1_RNASeq_10-sc-2133727" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784433</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_10-sc-2133727</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX662556">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662556</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904953, constructed from sample accession ERS554178 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence ACTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554178" refname="ZMP_phenotype_114_1_RNASeq_11-sc-2133728" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784434</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_11-sc-2133728</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX662557">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662557</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904931, constructed from sample accession ERS554156 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554156" refname="ZMP_phenotype_111_1_RNASeq_1-sc-2133706" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784412</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_1-sc-2133706</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX662558">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662558</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904932, constructed from sample accession ERS554157 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554157" refname="ZMP_phenotype_111_1_RNASeq_2-sc-2133707" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784413</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_2-sc-2133707</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX662559">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662559</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904933, constructed from sample accession ERS554158 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554158" refname="ZMP_phenotype_111_1_RNASeq_3-sc-2133708" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784414</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_3-sc-2133708</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX662560">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662560</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904934, constructed from sample accession ERS554159 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554159" refname="ZMP_phenotype_111_1_RNASeq_4-sc-2133709" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784415</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_4-sc-2133709</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904934</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX662561">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662561</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904935, constructed from sample accession ERS554160 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554160" refname="ZMP_phenotype_111_1_RNASeq_5-sc-2133710" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784416</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_5-sc-2133710</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904935</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX662562">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662562</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904936, constructed from sample accession ERS554161 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554161" refname="ZMP_phenotype_111_1_RNASeq_6-sc-2133711" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784417</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_6-sc-2133711</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX662563">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662563</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904937, constructed from sample accession ERS554162 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554162" refname="ZMP_phenotype_111_1_RNASeq_7-sc-2133712" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784418</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_7-sc-2133712</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX662564">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662564</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904938, constructed from sample accession ERS554163 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554163" refname="ZMP_phenotype_111_1_RNASeq_8-sc-2133713" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784419</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_8-sc-2133713</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX662565">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662565</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904939, constructed from sample accession ERS554164 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554164" refname="ZMP_phenotype_111_1_RNASeq_9-sc-2133714" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784420</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_9-sc-2133714</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX662566">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662566</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904940, constructed from sample accession ERS554165 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554165" refname="ZMP_phenotype_111_1_RNASeq_10-sc-2133715" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784421</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_10-sc-2133715</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX662567">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662567</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904941, constructed from sample accession ERS554166 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554166" refname="ZMP_phenotype_111_1_RNASeq_11-sc-2133716" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784422</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_11-sc-2133716</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904941</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX662568">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662568</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904942, constructed from sample accession ERS554167 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554167" refname="ZMP_phenotype_111_1_RNASeq_12-sc-2133717" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784423</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_12-sc-2133717</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX662569">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662569</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904943, constructed from sample accession ERS554168 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence AGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554168" refname="ZMP_phenotype_114_1_RNASeq_1-sc-2133718" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784424</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_1-sc-2133718</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX662570">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662570</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904944, constructed from sample accession ERS554169 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence AGTTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554169" refname="ZMP_phenotype_114_1_RNASeq_2-sc-2133719" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784425</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_2-sc-2133719</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904944</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX662571">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662571</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904945, constructed from sample accession ERS554170 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence ATGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554170" refname="ZMP_phenotype_114_1_RNASeq_3-sc-2133720" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554170</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784426</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_3-sc-2133720</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904945</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX662572">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662572</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904946, constructed from sample accession ERS554171 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence CCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554171" refname="ZMP_phenotype_114_1_RNASeq_4-sc-2133721" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554171</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784427</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_4-sc-2133721</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX662573">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662573</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904947, constructed from sample accession ERS554172 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554172" refname="ZMP_phenotype_114_1_RNASeq_5-sc-2133722" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554172</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784428</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_5-sc-2133722</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX662574">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662574</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904948, constructed from sample accession ERS554173 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554173" refname="ZMP_phenotype_114_1_RNASeq_6-sc-2133723" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554173</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784429</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_6-sc-2133723</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX662575">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662575</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904949, constructed from sample accession ERS554174 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GTGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554174" refname="ZMP_phenotype_114_1_RNASeq_7-sc-2133724" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554174</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784430</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_7-sc-2133724</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX662576">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904950, constructed from sample accession ERS554175 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554175" refname="ZMP_phenotype_114_1_RNASeq_8-sc-2133725" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554175</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784431</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_8-sc-2133725</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX662577">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904951, constructed from sample accession ERS554176 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence CGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554176" refname="ZMP_phenotype_114_1_RNASeq_9-sc-2133726" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554176</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784432</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_9-sc-2133726</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904951</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX662578">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904952, constructed from sample accession ERS554177 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence GAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554177" refname="ZMP_phenotype_114_1_RNASeq_10-sc-2133727" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554177</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784433</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_10-sc-2133727</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX662579">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904953, constructed from sample accession ERS554178 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_2).  This submission includes reads tagged with the sequence ACTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554178" refname="ZMP_phenotype_114_1_RNASeq_11-sc-2133728" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554178</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784434</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_11-sc-2133728</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX662486">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662486</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904907, constructed from sample accession ERS554132 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554132" refname="ZMP_phenotype_97_1_RNASeq_1-sc-2133682" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784388</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_1-sc-2133682</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX662487">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662487</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904908, constructed from sample accession ERS554133 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554133" refname="ZMP_phenotype_97_1_RNASeq_2-sc-2133683" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784389</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_2-sc-2133683</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX662488">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662488</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904909, constructed from sample accession ERS554134 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554134" refname="ZMP_phenotype_97_1_RNASeq_3-sc-2133684" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784390</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_3-sc-2133684</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX662489">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662489</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904910, constructed from sample accession ERS554135 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554135" refname="ZMP_phenotype_97_1_RNASeq_4-sc-2133685" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784391</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_4-sc-2133685</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX662490">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662490</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904911, constructed from sample accession ERS554136 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554136" refname="ZMP_phenotype_97_1_RNASeq_5-sc-2133686" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784392</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_5-sc-2133686</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904911</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX662491">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662491</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904912, constructed from sample accession ERS554137 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554137" refname="ZMP_phenotype_97_1_RNASeq_6-sc-2133687" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784393</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_6-sc-2133687</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX662492">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662492</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904913, constructed from sample accession ERS554138 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554138" refname="ZMP_phenotype_97_1_RNASeq_7-sc-2133688" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784394</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_7-sc-2133688</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX662493">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662493</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904914, constructed from sample accession ERS554139 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554139" refname="ZMP_phenotype_97_1_RNASeq_8-sc-2133689" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784395</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_8-sc-2133689</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904914</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX662494">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662494</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904915, constructed from sample accession ERS554140 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554140" refname="ZMP_phenotype_97_1_RNASeq_9-sc-2133690" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784396</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_9-sc-2133690</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904915</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX662495">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662495</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904916, constructed from sample accession ERS554141 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554141" refname="ZMP_phenotype_97_1_RNASeq_10-sc-2133691" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784397</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_10-sc-2133691</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX662496">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662496</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904917, constructed from sample accession ERS554142 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554142" refname="ZMP_phenotype_97_1_RNASeq_11-sc-2133692" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784398</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_11-sc-2133692</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX662497">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662497</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904918, constructed from sample accession ERS554143 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554143" refname="ZMP_phenotype_97_1_RNASeq_12-sc-2133693" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784399</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_12-sc-2133693</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX662498">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662498</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904919, constructed from sample accession ERS554144 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence AGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554144" refname="ZMP_phenotype_108_1_RNASeq_1-sc-2133694" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784400</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_1-sc-2133694</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX662499">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662499</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904920, constructed from sample accession ERS554145 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence AGTTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554145" refname="ZMP_phenotype_108_1_RNASeq_2-sc-2133695" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784401</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_2-sc-2133695</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX662500">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662500</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904921, constructed from sample accession ERS554146 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ATGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554146" refname="ZMP_phenotype_108_1_RNASeq_3-sc-2133696" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784402</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_3-sc-2133696</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX662501">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662501</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904922, constructed from sample accession ERS554147 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence CCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554147" refname="ZMP_phenotype_108_1_RNASeq_4-sc-2133697" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784403</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_4-sc-2133697</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX662502">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662502</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904923, constructed from sample accession ERS554148 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554148" refname="ZMP_phenotype_108_1_RNASeq_5-sc-2133698" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784404</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_5-sc-2133698</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX662503">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662503</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904924, constructed from sample accession ERS554149 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554149" refname="ZMP_phenotype_108_1_RNASeq_6-sc-2133699" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784405</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_6-sc-2133699</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX662504">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662504</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904925, constructed from sample accession ERS554150 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GTGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554150" refname="ZMP_phenotype_108_1_RNASeq_7-sc-2133700" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784406</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_7-sc-2133700</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904925</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX662505">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662505</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904926, constructed from sample accession ERS554151 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554151" refname="ZMP_phenotype_108_1_RNASeq_8-sc-2133701" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784407</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_8-sc-2133701</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX662506">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662506</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904927, constructed from sample accession ERS554152 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence CGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554152" refname="ZMP_phenotype_108_1_RNASeq_9-sc-2133702" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784408</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_9-sc-2133702</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX662507">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662507</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904928, constructed from sample accession ERS554153 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence GAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554153" refname="ZMP_phenotype_108_1_RNASeq_10-sc-2133703" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784409</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_10-sc-2133703</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX662508">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662508</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904929, constructed from sample accession ERS554154 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ACTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554154" refname="ZMP_phenotype_108_1_RNASeq_11-sc-2133704" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784410</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_11-sc-2133704</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_1#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX662509">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662509</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904930, constructed from sample accession ERS554155 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_1).  This submission includes reads tagged with the sequence ATTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554155" refname="ZMP_phenotype_108_1_RNASeq_12-sc-2133705" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784411</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_12-sc-2133705</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX662510">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662510</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904907, constructed from sample accession ERS554132 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554132" refname="ZMP_phenotype_97_1_RNASeq_1-sc-2133682" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554132</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784388</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_1-sc-2133682</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX662511">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662511</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904908, constructed from sample accession ERS554133 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554133" refname="ZMP_phenotype_97_1_RNASeq_2-sc-2133683" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554133</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784389</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_2-sc-2133683</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX662512">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662512</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904909, constructed from sample accession ERS554134 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554134" refname="ZMP_phenotype_97_1_RNASeq_3-sc-2133684" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554134</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784390</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_3-sc-2133684</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX662513">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662513</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904910, constructed from sample accession ERS554135 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554135" refname="ZMP_phenotype_97_1_RNASeq_4-sc-2133685" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554135</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784391</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_4-sc-2133685</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX662514">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662514</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904911, constructed from sample accession ERS554136 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554136" refname="ZMP_phenotype_97_1_RNASeq_5-sc-2133686" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554136</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784392</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_5-sc-2133686</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904911</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX662515">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662515</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904912, constructed from sample accession ERS554137 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554137" refname="ZMP_phenotype_97_1_RNASeq_6-sc-2133687" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554137</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784393</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_6-sc-2133687</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX662516">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662516</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904913, constructed from sample accession ERS554138 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554138" refname="ZMP_phenotype_97_1_RNASeq_7-sc-2133688" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554138</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784394</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_7-sc-2133688</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX662517">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662517</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904914, constructed from sample accession ERS554139 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554139" refname="ZMP_phenotype_97_1_RNASeq_8-sc-2133689" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554139</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784395</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_8-sc-2133689</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904914</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX662518">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662518</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904915, constructed from sample accession ERS554140 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554140" refname="ZMP_phenotype_97_1_RNASeq_9-sc-2133690" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554140</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784396</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_9-sc-2133690</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904915</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX662519">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662519</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904916, constructed from sample accession ERS554141 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554141" refname="ZMP_phenotype_97_1_RNASeq_10-sc-2133691" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554141</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784397</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_10-sc-2133691</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX662520">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662520</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904917, constructed from sample accession ERS554142 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554142" refname="ZMP_phenotype_97_1_RNASeq_11-sc-2133692" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554142</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784398</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_11-sc-2133692</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX662521">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662521</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904918, constructed from sample accession ERS554143 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554143" refname="ZMP_phenotype_97_1_RNASeq_12-sc-2133693" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554143</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784399</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_97_1_RNASeq_12-sc-2133693</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX662522">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662522</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904919, constructed from sample accession ERS554144 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence AGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554144" refname="ZMP_phenotype_108_1_RNASeq_1-sc-2133694" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554144</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784400</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_1-sc-2133694</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX662523">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662523</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904920, constructed from sample accession ERS554145 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence AGTTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554145" refname="ZMP_phenotype_108_1_RNASeq_2-sc-2133695" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554145</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784401</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_2-sc-2133695</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX662524">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904921, constructed from sample accession ERS554146 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ATGTCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554146" refname="ZMP_phenotype_108_1_RNASeq_3-sc-2133696" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554146</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784402</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_3-sc-2133696</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX662525">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904922, constructed from sample accession ERS554147 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence CCGTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554147" refname="ZMP_phenotype_108_1_RNASeq_4-sc-2133697" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554147</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784403</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_4-sc-2133697</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX662526">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904923, constructed from sample accession ERS554148 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GTCCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554148" refname="ZMP_phenotype_108_1_RNASeq_5-sc-2133698" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554148</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784404</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_5-sc-2133698</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX662527">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904924, constructed from sample accession ERS554149 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GTGAAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554149" refname="ZMP_phenotype_108_1_RNASeq_6-sc-2133699" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554149</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784405</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_6-sc-2133699</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX662528">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904925, constructed from sample accession ERS554150 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GTGGCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554150" refname="ZMP_phenotype_108_1_RNASeq_7-sc-2133700" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554150</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784406</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_7-sc-2133700</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904925</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX662529">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662529</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904926, constructed from sample accession ERS554151 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GTTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554151" refname="ZMP_phenotype_108_1_RNASeq_8-sc-2133701" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554151</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784407</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_8-sc-2133701</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX662530">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662530</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904927, constructed from sample accession ERS554152 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence CGTACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554152" refname="ZMP_phenotype_108_1_RNASeq_9-sc-2133702" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554152</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784408</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_9-sc-2133702</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX662531">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662531</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904928, constructed from sample accession ERS554153 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence GAGTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554153" refname="ZMP_phenotype_108_1_RNASeq_10-sc-2133703" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554153</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784409</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_10-sc-2133703</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX662532">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662532</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904929, constructed from sample accession ERS554154 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ACTGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554154" refname="ZMP_phenotype_108_1_RNASeq_11-sc-2133704" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554154</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784410</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_11-sc-2133704</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14260_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX662533">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662533</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14260_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14260_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904930, constructed from sample accession ERS554155 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14260_2).  This submission includes reads tagged with the sequence ATTCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554155" refname="ZMP_phenotype_108_1_RNASeq_12-sc-2133705" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554155</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784411</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_108_1_RNASeq_12-sc-2133705</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX662534">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662534</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904931, constructed from sample accession ERS554156 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence ATCACG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554156" refname="ZMP_phenotype_111_1_RNASeq_1-sc-2133706" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554156</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784412</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_1-sc-2133706</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX662535">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662535</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904932, constructed from sample accession ERS554157 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence CGATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554157" refname="ZMP_phenotype_111_1_RNASeq_2-sc-2133707" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554157</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784413</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_2-sc-2133707</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX662536">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662536</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904933, constructed from sample accession ERS554158 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence TTAGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554158" refname="ZMP_phenotype_111_1_RNASeq_3-sc-2133708" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554158</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784414</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_3-sc-2133708</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX662537">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662537</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904934, constructed from sample accession ERS554159 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence TGACCA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554159" refname="ZMP_phenotype_111_1_RNASeq_4-sc-2133709" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554159</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784415</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_4-sc-2133709</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904934</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX662538">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662538</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904935, constructed from sample accession ERS554160 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence ACAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554160" refname="ZMP_phenotype_111_1_RNASeq_5-sc-2133710" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554160</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784416</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_5-sc-2133710</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904935</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX662539">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662539</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904936, constructed from sample accession ERS554161 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GCCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554161" refname="ZMP_phenotype_111_1_RNASeq_6-sc-2133711" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554161</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784417</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_6-sc-2133711</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX662540">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662540</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904937, constructed from sample accession ERS554162 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence CAGATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554162" refname="ZMP_phenotype_111_1_RNASeq_7-sc-2133712" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554162</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784418</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_7-sc-2133712</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX662541">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662541</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904938, constructed from sample accession ERS554163 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence ACTTGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554163" refname="ZMP_phenotype_111_1_RNASeq_8-sc-2133713" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554163</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784419</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_8-sc-2133713</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX662542">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662542</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904939, constructed from sample accession ERS554164 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GATCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554164" refname="ZMP_phenotype_111_1_RNASeq_9-sc-2133714" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554164</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784420</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_9-sc-2133714</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX662543">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662543</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904940, constructed from sample accession ERS554165 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence TAGCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554165" refname="ZMP_phenotype_111_1_RNASeq_10-sc-2133715" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554165</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784421</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_10-sc-2133715</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX662544">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662544</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904941, constructed from sample accession ERS554166 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence GGCTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554166" refname="ZMP_phenotype_111_1_RNASeq_11-sc-2133716" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554166</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784422</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_11-sc-2133716</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904941</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX662545">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662545</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904942, constructed from sample accession ERS554167 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence CTTGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554167" refname="ZMP_phenotype_111_1_RNASeq_12-sc-2133717" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554167</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784423</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_111_1_RNASeq_12-sc-2133717</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX662546">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662546</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904943, constructed from sample accession ERS554168 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence AGTCAA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554168" refname="ZMP_phenotype_114_1_RNASeq_1-sc-2133718" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554168</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784424</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_1-sc-2133718</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_14262_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX662547">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX662547</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_14262_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_14262_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP007082" refname="Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP007082</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Transcriptome_profiling_of_mutants_from_the_zebrafish_mutation_project-sc-3313</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 11904944, constructed from sample accession ERS554169 for study accession ERP007082.  This is part of an Illumina multiplexed sequencing run (14262_1).  This submission includes reads tagged with the sequence AGTTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS554169" refname="ZMP_phenotype_114_1_RNASeq_2-sc-2133719" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS554169</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2784425</EXTERNAL_ID>
          <SUBMITTER_ID namespace="SC">ZMP_phenotype_114_1_RNASeq_2-sc-2133719</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>11904944</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="170"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
