<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_16022_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045012">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045012</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477742, constructed from sample accession ERS700766 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700766" refname="0_5BRAF_0_1DMSO_28hpf_treated_1-sc-2268051" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700766</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_1-sc-2268051</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477742</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045013">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045013</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477743, constructed from sample accession ERS700767 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700767" refname="0_5BRAF_0_1DMSO_28hpf_treated_3-sc-2268052" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700767</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_3-sc-2268052</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477743</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045014">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477744, constructed from sample accession ERS700768 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700768" refname="0_5BRAF_0_1DMSO_28hpf_treated_4-sc-2268053" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700768</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_4-sc-2268053</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477744</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045015">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045015</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477745, constructed from sample accession ERS700769 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700769" refname="0_5BRAF_0_1DMSO_28hpf_treated_5-sc-2268054" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700769</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_5-sc-2268054</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477745</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045016">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477746, constructed from sample accession ERS700770 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700770" refname="0_5BRAF_0_1DMSO_28hpf_treated_6-sc-2268055" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700770</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_6-sc-2268055</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477746</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045017">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477747, constructed from sample accession ERS700771 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700771" refname="0_5BRAF_0_1DMSO_28hpf_treated_7-sc-2268056" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700771</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_7-sc-2268056</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477747</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477748, constructed from sample accession ERS700772 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700772" refname="0_5BRAF_0_1DMSO_28hpf_treated_8-sc-2268057" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700772</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_8-sc-2268057</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477748</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045019">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045019</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477749, constructed from sample accession ERS700773 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700773" refname="0_5BRAF_0_1DMSO_28hpf_treated_9-sc-2268058" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700773</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_9-sc-2268058</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477749</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045020">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045020</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477750, constructed from sample accession ERS700774 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700774" refname="0_5BRAF_0_1DMSO_28hpf_treated_10-sc-2268059" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700774</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_10-sc-2268059</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477750</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045021">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045021</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477751, constructed from sample accession ERS700775 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700775" refname="0_5BRAF_0_1DMSO_28hpf_treated_11-sc-2268060" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700775</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_11-sc-2268060</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477751</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045022">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045022</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477752, constructed from sample accession ERS700776 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700776" refname="0_5BRAF_0_1DMSO_28hpf_treated_12-sc-2268061" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700776</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_12-sc-2268061</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477752</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045023">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045023</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477753, constructed from sample accession ERS700777 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700777" refname="1BRAF_0_1DMSO_28hpf_treated_1-sc-2268062" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700777</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_1-sc-2268062</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477753</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045024">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045024</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477754, constructed from sample accession ERS700778 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700778" refname="1BRAF_0_1DMSO_28hpf_treated_2-sc-2268063" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700778</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_2-sc-2268063</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477754</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045025">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477755, constructed from sample accession ERS700779 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700779" refname="1BRAF_0_1DMSO_28hpf_treated_3-sc-2268064" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700779</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_3-sc-2268064</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477755</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045026">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477756, constructed from sample accession ERS700780 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700780" refname="1BRAF_0_1DMSO_28hpf_treated_4-sc-2268065" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700780</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_4-sc-2268065</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477756</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045027">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477757, constructed from sample accession ERS700781 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700781" refname="1BRAF_0_1DMSO_28hpf_treated_5-sc-2268066" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700781</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_5-sc-2268066</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477757</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045028">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477758, constructed from sample accession ERS700782 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700782" refname="1BRAF_0_1DMSO_28hpf_treated_6-sc-2268067" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700782</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_6-sc-2268067</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477758</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045029">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477759, constructed from sample accession ERS700783 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700783" refname="1BRAF_0_1DMSO_28hpf_treated_7-sc-2268068" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700783</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_7-sc-2268068</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477759</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045030">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477760, constructed from sample accession ERS700784 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700784" refname="1BRAF_0_1DMSO_28hpf_treated_8-sc-2268069" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700784</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_8-sc-2268069</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477760</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045031">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477761, constructed from sample accession ERS700785 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700785" refname="1BRAF_0_1DMSO_28hpf_treated_9-sc-2268070" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700785</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_9-sc-2268070</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477761</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045032">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477762, constructed from sample accession ERS700786 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700786" refname="1BRAF_0_1DMSO_28hpf_treated_10-sc-2268071" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700786</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_10-sc-2268071</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477762</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045033">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477763, constructed from sample accession ERS700787 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700787" refname="1BRAF_0_1DMSO_28hpf_treated_11-sc-2268072" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700787</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_11-sc-2268072</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477763</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045034">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477764, constructed from sample accession ERS700788 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700788" refname="1BRAF_0_1DMSO_28hpf_treated_12-sc-2268073" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700788</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_12-sc-2268073</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477764</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045035">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477765, constructed from sample accession ERS700789 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700789" refname="2BRAF_0_1DMSO_28hpf_treated_1-sc-2268074" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700789</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_1-sc-2268074</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477765</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045036">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045036</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477766, constructed from sample accession ERS700790 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700790" refname="2BRAF_0_1DMSO_28hpf_treated_2-sc-2268075" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700790</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_2-sc-2268075</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477766</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045037">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045037</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477767, constructed from sample accession ERS700791 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700791" refname="2BRAF_0_1DMSO_28hpf_treated_3-sc-2268076" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700791</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_3-sc-2268076</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477767</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045038">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045038</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477768, constructed from sample accession ERS700792 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700792" refname="2BRAF_0_1DMSO_28hpf_treated_4-sc-2268077" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700792</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_4-sc-2268077</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477768</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045039">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045039</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477769, constructed from sample accession ERS700793 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700793" refname="2BRAF_0_1DMSO_28hpf_treated_5-sc-2268078" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700793</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_5-sc-2268078</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477769</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045040">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045040</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477770, constructed from sample accession ERS700794 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700794" refname="2BRAF_0_1DMSO_28hpf_treated_6-sc-2268079" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700794</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_6-sc-2268079</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477770</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045041">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045041</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477771, constructed from sample accession ERS700795 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700795" refname="2BRAF_0_1DMSO_28hpf_treated_7-sc-2268080" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700795</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_7-sc-2268080</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477771</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045042">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045042</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477772, constructed from sample accession ERS700796 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700796" refname="2BRAF_0_1DMSO_28hpf_treated_8-sc-2268081" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700796</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_8-sc-2268081</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477772</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045043">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045043</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477773, constructed from sample accession ERS700797 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700797" refname="2BRAF_0_1DMSO_28hpf_treated_9-sc-2268082" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700797</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_9-sc-2268082</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477773</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045044">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045044</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477774, constructed from sample accession ERS700798 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700798" refname="2BRAF_0_1DMSO_28hpf_treated_10-sc-2268083" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700798</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_10-sc-2268083</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477774</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045045">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045045</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477775, constructed from sample accession ERS700799 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700799" refname="2BRAF_0_1DMSO_28hpf_treated_11-sc-2268084" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700799</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_11-sc-2268084</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477775</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045046">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045046</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477776, constructed from sample accession ERS700800 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700800" refname="2BRAF_0_1DMSO_28hpf_treated_12-sc-2268085" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700800</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_12-sc-2268085</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477776</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045047">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045047</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477777, constructed from sample accession ERS700801 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700801" refname="BRAF_0_1DMSO_28hpf_control_1-sc-2268086" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700801</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_1-sc-2268086</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477777</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045048">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045048</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477778, constructed from sample accession ERS700802 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700802" refname="BRAF_0_1DMSO_28hpf_control_2-sc-2268087" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700802</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_2-sc-2268087</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477778</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045049">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045049</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477779, constructed from sample accession ERS700803 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700803" refname="BRAF_0_1DMSO_28hpf_control_3-sc-2268088" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700803</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_3-sc-2268088</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477779</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045050">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045050</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477780, constructed from sample accession ERS700804 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700804" refname="BRAF_0_1DMSO_28hpf_control_4-sc-2268089" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700804</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_4-sc-2268089</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477780</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045051">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045051</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477781, constructed from sample accession ERS700805 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700805" refname="BRAF_0_1DMSO_28hpf_control_5-sc-2268090" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700805</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_5-sc-2268090</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477781</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045052">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045052</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477782, constructed from sample accession ERS700806 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700806" refname="BRAF_0_1DMSO_28hpf_control_6-sc-2268091" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700806</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_6-sc-2268091</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477782</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045053">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045053</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477783, constructed from sample accession ERS700807 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700807" refname="BRAF_0_1DMSO_28hpf_control_7-sc-2268092" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700807</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_7-sc-2268092</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477783</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045054">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045054</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477784, constructed from sample accession ERS700808 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700808" refname="BRAF_0_1DMSO_28hpf_control_8-sc-2268093" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700808</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_8-sc-2268093</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477784</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045055">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045055</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477785, constructed from sample accession ERS700809 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700809" refname="BRAF_0_1DMSO_28hpf_control_9-sc-2268094" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700809</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_9-sc-2268094</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477785</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045056">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045056</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477786, constructed from sample accession ERS700810 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700810" refname="BRAF_0_1DMSO_28hpf_control_10-sc-2268095" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700810</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_10-sc-2268095</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477786</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045057">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045057</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477787, constructed from sample accession ERS700811 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700811" refname="BRAF_0_1DMSO_28hpf_control_11-sc-2268096" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700811</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_11-sc-2268096</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477787</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045058">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045058</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477788, constructed from sample accession ERS700812 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700812" refname="BRAF_0_1DMSO_28hpf_control_12-sc-2268097" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700812</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_12-sc-2268097</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477788</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045059">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045059</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477789, constructed from sample accession ERS700813 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700813" refname="BRAF_0_1DMSO_28hpf_untreated_1-sc-2268098" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700813</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_1-sc-2268098</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477789</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045060">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045060</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477790, constructed from sample accession ERS700814 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700814" refname="BRAF_0_1DMSO_28hpf_untreated_2-sc-2268099" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700814</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_2-sc-2268099</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477790</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045061">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045061</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477791, constructed from sample accession ERS700815 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700815" refname="BRAF_0_1DMSO_28hpf_untreated_3-sc-2268100" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700815</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_3-sc-2268100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477791</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045062">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045062</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477792, constructed from sample accession ERS700816 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700816" refname="BRAF_0_1DMSO_28hpf_untreated_4-sc-2268101" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700816</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_4-sc-2268101</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477792</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045063">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045063</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477793, constructed from sample accession ERS700817 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700817" refname="BRAF_0_1DMSO_28hpf_untreated_6-sc-2268102" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700817</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_6-sc-2268102</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477793</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045064">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045064</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477794, constructed from sample accession ERS700818 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700818" refname="BRAF_0_1DMSO_28hpf_untreated_7-sc-2268103" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700818</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_7-sc-2268103</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477794</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045065">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045065</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477795, constructed from sample accession ERS700819 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700819" refname="BRAF_0_1DMSO_28hpf_untreated_8-sc-2268104" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700819</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_8-sc-2268104</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477795</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045066">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045066</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477796, constructed from sample accession ERS700820 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700820" refname="BRAF_0_1DMSO_28hpf_untreated_9-sc-2268105" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700820</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_9-sc-2268105</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477796</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045067">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045067</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477797, constructed from sample accession ERS700821 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700821" refname="BRAF_0_1DMSO_28hpf_untreated_10-sc-2268106" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700821</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_10-sc-2268106</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477797</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045068">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045068</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477798, constructed from sample accession ERS700822 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700822" refname="BRAF_0_1DMSO_28hpf_untreated_11-sc-2268107" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700822</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_11-sc-2268107</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477798</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_1#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045069">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045069</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_1#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_1#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477799, constructed from sample accession ERS700823 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_1).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700823" refname="BRAF_0_1DMSO_28hpf_untreated_12-sc-2268108" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700823</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_12-sc-2268108</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477799</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045070">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045070</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477742, constructed from sample accession ERS700766 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence ATCACGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700766" refname="0_5BRAF_0_1DMSO_28hpf_treated_1-sc-2268051" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700766</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_1-sc-2268051</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477742</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045071">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045071</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477743, constructed from sample accession ERS700767 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTAGGCAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700767" refname="0_5BRAF_0_1DMSO_28hpf_treated_3-sc-2268052" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700767</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_3-sc-2268052</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477743</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045072">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045072</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477744, constructed from sample accession ERS700768 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGACCACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700768" refname="0_5BRAF_0_1DMSO_28hpf_treated_4-sc-2268053" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700768</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_4-sc-2268053</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477744</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045073">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045073</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477745, constructed from sample accession ERS700769 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence ACAGTGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700769" refname="0_5BRAF_0_1DMSO_28hpf_treated_5-sc-2268054" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700769</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_5-sc-2268054</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477745</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045074">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045074</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477746, constructed from sample accession ERS700770 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence GCCAATGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700770" refname="0_5BRAF_0_1DMSO_28hpf_treated_6-sc-2268055" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700770</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_6-sc-2268055</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477746</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#6" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045075">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045075</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#6</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477747, constructed from sample accession ERS700771 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence CAGATCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700771" refname="0_5BRAF_0_1DMSO_28hpf_treated_7-sc-2268056" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700771</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_7-sc-2268056</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477747</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045076">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045076</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477748, constructed from sample accession ERS700772 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence ACTTGATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700772" refname="0_5BRAF_0_1DMSO_28hpf_treated_8-sc-2268057" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700772</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_8-sc-2268057</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477748</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045077">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045077</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477749, constructed from sample accession ERS700773 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence GATCAGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700773" refname="0_5BRAF_0_1DMSO_28hpf_treated_9-sc-2268058" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700773</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_9-sc-2268058</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477749</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#9" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045078">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045078</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#9</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477750, constructed from sample accession ERS700774 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAGCTTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700774" refname="0_5BRAF_0_1DMSO_28hpf_treated_10-sc-2268059" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700774</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_10-sc-2268059</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477750</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#10" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045079">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045079</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#10</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477751, constructed from sample accession ERS700775 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence GGCTACAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700775" refname="0_5BRAF_0_1DMSO_28hpf_treated_11-sc-2268060" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700775</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_11-sc-2268060</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477751</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#11" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045080">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045080</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#11</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477752, constructed from sample accession ERS700776 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence CTTGTACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700776" refname="0_5BRAF_0_1DMSO_28hpf_treated_12-sc-2268061" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700776</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">0_5BRAF_0_1DMSO_28hpf_treated_12-sc-2268061</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477752</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#12" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045081">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045081</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#12</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#12</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477753, constructed from sample accession ERS700777 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGGTTGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700777" refname="1BRAF_0_1DMSO_28hpf_treated_1-sc-2268062" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700777</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_1-sc-2268062</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477753</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045082">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045082</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477754, constructed from sample accession ERS700778 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCTCGGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700778" refname="1BRAF_0_1DMSO_28hpf_treated_2-sc-2268063" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700778</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_2-sc-2268063</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477754</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045083">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045083</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477755, constructed from sample accession ERS700779 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAAGCGTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700779" refname="1BRAF_0_1DMSO_28hpf_treated_3-sc-2268064" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700779</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_3-sc-2268064</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477755</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045084">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045084</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477756, constructed from sample accession ERS700780 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCCGTCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700780" refname="1BRAF_0_1DMSO_28hpf_treated_4-sc-2268065" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700780</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_4-sc-2268065</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477756</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045085">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045085</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477757, constructed from sample accession ERS700781 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGTACCTT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700781" refname="1BRAF_0_1DMSO_28hpf_treated_5-sc-2268066" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700781</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_5-sc-2268066</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477757</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045086">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045086</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477758, constructed from sample accession ERS700782 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTCTGTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700782" refname="1BRAF_0_1DMSO_28hpf_treated_6-sc-2268067" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700782</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_6-sc-2268067</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477758</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#18" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045087">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045087</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#18</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477759, constructed from sample accession ERS700783 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCTGCTGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700783" refname="1BRAF_0_1DMSO_28hpf_treated_7-sc-2268068" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700783</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_7-sc-2268068</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477759</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045088">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045088</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477760, constructed from sample accession ERS700784 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTGGAGGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700784" refname="1BRAF_0_1DMSO_28hpf_treated_8-sc-2268069" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700784</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_8-sc-2268069</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477760</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045089">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045089</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477761, constructed from sample accession ERS700785 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCGAGCGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700785" refname="1BRAF_0_1DMSO_28hpf_treated_9-sc-2268070" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700785</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_9-sc-2268070</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477761</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#21" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045090">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045090</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#21</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477762, constructed from sample accession ERS700786 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGATACGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700786" refname="1BRAF_0_1DMSO_28hpf_treated_10-sc-2268071" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700786</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_10-sc-2268071</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477762</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#22" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045091">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045091</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#22</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477763, constructed from sample accession ERS700787 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGCATAGT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700787" refname="1BRAF_0_1DMSO_28hpf_treated_11-sc-2268072" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700787</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_11-sc-2268072</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477763</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#23" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045092">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045092</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#23</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477764, constructed from sample accession ERS700788 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTGACTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700788" refname="1BRAF_0_1DMSO_28hpf_treated_12-sc-2268073" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700788</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">1BRAF_0_1DMSO_28hpf_treated_12-sc-2268073</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477764</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#24" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045093">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045093</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#24</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#24</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477765, constructed from sample accession ERS700789 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGCGATCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700789" refname="2BRAF_0_1DMSO_28hpf_treated_1-sc-2268074" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700789</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_1-sc-2268074</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477765</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045094">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045094</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477766, constructed from sample accession ERS700790 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTCCTGCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700790" refname="2BRAF_0_1DMSO_28hpf_treated_2-sc-2268075" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700790</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_2-sc-2268075</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477766</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045095">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045095</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477767, constructed from sample accession ERS700791 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAGTGACT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700791" refname="2BRAF_0_1DMSO_28hpf_treated_3-sc-2268076" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700791</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_3-sc-2268076</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477767</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045096">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045096</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477768, constructed from sample accession ERS700792 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TACAGGAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700792" refname="2BRAF_0_1DMSO_28hpf_treated_4-sc-2268077" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700792</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_4-sc-2268077</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477768</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045097">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045097</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477769, constructed from sample accession ERS700793 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCCTCAAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700793" refname="2BRAF_0_1DMSO_28hpf_treated_5-sc-2268078" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700793</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_5-sc-2268078</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477769</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045098">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045098</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477770, constructed from sample accession ERS700794 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGTGGTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700794" refname="2BRAF_0_1DMSO_28hpf_treated_6-sc-2268079" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700794</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_6-sc-2268079</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477770</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#30" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045099">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045099</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#30</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#30</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477771, constructed from sample accession ERS700795 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAGTCTTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700795" refname="2BRAF_0_1DMSO_28hpf_treated_7-sc-2268080" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700795</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_7-sc-2268080</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477771</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045100</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477772, constructed from sample accession ERS700796 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTCCATTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700796" refname="2BRAF_0_1DMSO_28hpf_treated_8-sc-2268081" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700796</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_8-sc-2268081</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477772</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045101</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477773, constructed from sample accession ERS700797 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCGAAGTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700797" refname="2BRAF_0_1DMSO_28hpf_treated_9-sc-2268082" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700797</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_9-sc-2268082</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477773</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#33" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045102</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#33</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#33</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477774, constructed from sample accession ERS700798 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAACGCTG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700798" refname="2BRAF_0_1DMSO_28hpf_treated_10-sc-2268083" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700798</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_10-sc-2268083</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477774</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#34" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045103</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#34</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#34</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477775, constructed from sample accession ERS700799 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTGGTATG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700799" refname="2BRAF_0_1DMSO_28hpf_treated_11-sc-2268084" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700799</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_11-sc-2268084</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477775</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#35" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045104">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045104</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#35</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#35</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477776, constructed from sample accession ERS700800 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGAACTGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700800" refname="2BRAF_0_1DMSO_28hpf_treated_12-sc-2268085" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700800</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">2BRAF_0_1DMSO_28hpf_treated_12-sc-2268085</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477776</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#36" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045105">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045105</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#36</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#36</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477777, constructed from sample accession ERS700801 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TACTTCGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700801" refname="BRAF_0_1DMSO_28hpf_control_1-sc-2268086" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700801</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_1-sc-2268086</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477777</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045106">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045106</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477778, constructed from sample accession ERS700802 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCTCACGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700802" refname="BRAF_0_1DMSO_28hpf_control_2-sc-2268087" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700802</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_2-sc-2268087</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477778</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045107">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045107</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477779, constructed from sample accession ERS700803 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCAGGAGG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700803" refname="BRAF_0_1DMSO_28hpf_control_3-sc-2268088" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700803</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_3-sc-2268088</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477779</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045108">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045108</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477780, constructed from sample accession ERS700804 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAAGTTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700804" refname="BRAF_0_1DMSO_28hpf_control_4-sc-2268089" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700804</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_4-sc-2268089</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477780</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045109">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045109</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477781, constructed from sample accession ERS700805 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCCAGTCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700805" refname="BRAF_0_1DMSO_28hpf_control_5-sc-2268090" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700805</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_5-sc-2268090</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477781</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045110">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045110</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477782, constructed from sample accession ERS700806 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGTATGCG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700806" refname="BRAF_0_1DMSO_28hpf_control_6-sc-2268091" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700806</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_6-sc-2268091</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477782</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#42" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045111">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045111</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#42</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#42</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477783, constructed from sample accession ERS700807 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCATTGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700807" refname="BRAF_0_1DMSO_28hpf_control_7-sc-2268092" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700807</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_7-sc-2268092</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477783</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045112">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045112</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477784, constructed from sample accession ERS700808 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGGCTCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700808" refname="BRAF_0_1DMSO_28hpf_control_8-sc-2268093" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700808</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_8-sc-2268093</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477784</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045113">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045113</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477785, constructed from sample accession ERS700809 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TATGCCAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700809" refname="BRAF_0_1DMSO_28hpf_control_9-sc-2268094" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700809</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_9-sc-2268094</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477785</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#45" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045114">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045114</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#45</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#45</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477786, constructed from sample accession ERS700810 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCAGATTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700810" refname="BRAF_0_1DMSO_28hpf_control_10-sc-2268095" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700810</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_10-sc-2268095</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477786</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#46" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045115">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045115</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#46</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#46</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477787, constructed from sample accession ERS700811 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TACTAGTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700811" refname="BRAF_0_1DMSO_28hpf_control_11-sc-2268096" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700811</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_11-sc-2268096</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477787</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#47" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045116">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045116</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#47</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#47</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477788, constructed from sample accession ERS700812 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTCAGCTC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700812" refname="BRAF_0_1DMSO_28hpf_control_12-sc-2268097" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700812</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_control_12-sc-2268097</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477788</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#48" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045117">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045117</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#48</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#48</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477789, constructed from sample accession ERS700813 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGTCTATC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700813" refname="BRAF_0_1DMSO_28hpf_untreated_1-sc-2268098" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700813</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_1-sc-2268098</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477789</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045118">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045118</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477790, constructed from sample accession ERS700814 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TATGTGGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700814" refname="BRAF_0_1DMSO_28hpf_untreated_2-sc-2268099" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700814</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_2-sc-2268099</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477790</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045119">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045119</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477791, constructed from sample accession ERS700815 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTACTCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700815" refname="BRAF_0_1DMSO_28hpf_untreated_3-sc-2268100" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700815</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_3-sc-2268100</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477791</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045120">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045120</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477792, constructed from sample accession ERS700816 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCGTTAGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700816" refname="BRAF_0_1DMSO_28hpf_untreated_4-sc-2268101" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700816</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_4-sc-2268101</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477792</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045121">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045121</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477793, constructed from sample accession ERS700817 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGTTCTCC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700817" refname="BRAF_0_1DMSO_28hpf_untreated_6-sc-2268102" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700817</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_6-sc-2268102</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477793</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045122">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045122</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477794, constructed from sample accession ERS700818 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTCGCACC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700818" refname="BRAF_0_1DMSO_28hpf_untreated_7-sc-2268103" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700818</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_7-sc-2268103</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477794</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#54" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045123">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045123</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#54</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#54</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477795, constructed from sample accession ERS700819 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TTGCGTAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700819" refname="BRAF_0_1DMSO_28hpf_untreated_8-sc-2268104" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700819</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_8-sc-2268104</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477795</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045124">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045124</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477796, constructed from sample accession ERS700820 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCTACGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700820" refname="BRAF_0_1DMSO_28hpf_untreated_9-sc-2268105" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700820</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_9-sc-2268105</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477796</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045125">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045125</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477797, constructed from sample accession ERS700821 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TGACAGAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700821" refname="BRAF_0_1DMSO_28hpf_untreated_10-sc-2268106" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700821</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_10-sc-2268106</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477797</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#57" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045126">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045126</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#57</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#57</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477798, constructed from sample accession ERS700822 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TAGAACAC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700822" refname="BRAF_0_1DMSO_28hpf_untreated_11-sc-2268107" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700822</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_11-sc-2268107</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477798</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_16022_2#58" center_name="The Wellcome Trust Sanger Institute" accession="ERX1045127">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX1045127</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_16022_2#58</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_16022_2#58</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP008536" refname="Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008536</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Screening_zebrafish_embryos_treated_with_small_molecules_by_transcriptome_profiling-sc-3143</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 13477799, constructed from sample accession ERS700823 for study accession ERP008536.  This is part of an Illumina multiplexed sequencing run (16022_2).  This submission includes reads tagged with the sequence TCATCCTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700823" refname="BRAF_0_1DMSO_28hpf_untreated_12-sc-2268108" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700823</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">BRAF_0_1DMSO_28hpf_untreated_12-sc-2268108</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>13477799</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>Transcriptome counting qPCR only</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
