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    <TITLE>GSM2858442: DMSO_1; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858443: BaP_10nM_1; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858444: BaP_1μM_1; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858445: EE2_10nM_1; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858447: DMSO_2; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858448: BaP_10nM_2; Gadus morhua; RNA-Seq</TITLE>
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    <TITLE>GSM2858451: Mix_10nM_2; Gadus morhua; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858451</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858451</ID>
          <LABEL>GSM2858451</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858451</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858452" accession="SRX3397824">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397824</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858452</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858452: Mix_1μM_2; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858452</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858452</ID>
          <LABEL>GSM2858452</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858452</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858453" accession="SRX3397825">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397825</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858453</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858453: DMSO_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858453</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858453</ID>
          <LABEL>GSM2858453</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858453</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858454" accession="SRX3397826">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397826</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858454</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858454: BaP_10nM_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858454</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858454</ID>
          <LABEL>GSM2858454</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858454</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858455" accession="SRX3397827">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397827</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858455</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858455: BaP_1μM_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858455</ID>
          <LABEL>GSM2858455</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858455</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858456" accession="SRX3397828">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397828</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858456: EE2_10nM_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858456</ID>
          <LABEL>GSM2858456</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858456</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858457" accession="SRX3397829">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397829</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858457: EE2_1μM_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858457</ID>
          <LABEL>GSM2858457</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858457</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858458" accession="SRX3397830">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397830</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858458: Mix_1μM_3; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858458</ID>
          <LABEL>GSM2858458</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858458</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858459" accession="SRX3397831">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397831</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858459: DMSO_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858459</ID>
          <LABEL>GSM2858459</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858459</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858460" accession="SRX3397832">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397832</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858460</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858460: BaP_10nM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858460</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858460</ID>
          <LABEL>GSM2858460</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858460</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858461" accession="SRX3397833">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397833</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858461</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858461: BaP_1μM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858461</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858461</ID>
          <LABEL>GSM2858461</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858461</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858462" accession="SRX3397834">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397834</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858462</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858462: EE2_10nM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858462</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858462</ID>
          <LABEL>GSM2858462</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858462</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858463" accession="SRX3397835">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397835</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858463</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858463: EE2_1μM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858463</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858463</ID>
          <LABEL>GSM2858463</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858463</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858464" accession="SRX3397836">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397836</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858464</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858464: Mix_10nM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692020">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692020</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858464</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858464</ID>
          <LABEL>GSM2858464</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858464</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858465" accession="SRX3397837">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397837</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858465</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858465: Mix_1μM_4; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692021">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692021</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858465</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858465</ID>
          <LABEL>GSM2858465</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858465</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858466" accession="SRX3397838">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397838</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858466</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858466: DMSO_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692022">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692022</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858466</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858466</ID>
          <LABEL>GSM2858466</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858466</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858467" accession="SRX3397839">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397839</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858467</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858467: BaP_10nM_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692023">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692023</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858467</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858467</ID>
          <LABEL>GSM2858467</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858467</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858468" accession="SRX3397840">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397840</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858468</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858468: BaP_1μM_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692024">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692024</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858468</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858468</ID>
          <LABEL>GSM2858468</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858468</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858469" accession="SRX3397841">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397841</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858469</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858469: EE2_1μM_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692025">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692025</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858469</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858469</ID>
          <LABEL>GSM2858469</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858469</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858470" accession="SRX3397842">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397842</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858470</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858470: Mix_10nM_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692026">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692026</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858470</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858470</ID>
          <LABEL>GSM2858470</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858470</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858471" accession="SRX3397843">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397843</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858471</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858471: Mix_1μM_5; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692027">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692027</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858471</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858471</ID>
          <LABEL>GSM2858471</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858471</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858472" accession="SRX3397844">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397844</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858472</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858472: DMSO_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692028">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692028</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858472</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858472</ID>
          <LABEL>GSM2858472</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858472</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858473" accession="SRX3397845">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397845</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858473</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858473: BaP_10nM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692029">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692029</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858473</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858473</ID>
          <LABEL>GSM2858473</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858473</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858474" accession="SRX3397846">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397846</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858474</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858474: BaP_1μM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692030">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692030</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858474</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858474</ID>
          <LABEL>GSM2858474</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858474</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858475" accession="SRX3397847">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397847</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858475</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858475: EE2_10nM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692031">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692031</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858475</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858475</ID>
          <LABEL>GSM2858475</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858475</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858476" accession="SRX3397848">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397848</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858476</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858476: EE2_1μM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692032">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692032</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858476</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858476</ID>
          <LABEL>GSM2858476</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858476</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858477" accession="SRX3397849">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397849</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858477</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858477: Mix_10nM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692033">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692033</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858477</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858477</ID>
          <LABEL>GSM2858477</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858477</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858478" accession="SRX3397850">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397850</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858478</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858478: Mix_1μM_6; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692034">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692034</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858478</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858478</ID>
          <LABEL>GSM2858478</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858478</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858479" accession="SRX3397851">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397851</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858479</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858479: DMSO_7; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692035">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692035</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858479</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858479</ID>
          <LABEL>GSM2858479</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858479</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858480" accession="SRX3397852">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397852</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858480</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858480: BaP_1μM_7; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692036">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692036</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858480</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858480</ID>
          <LABEL>GSM2858480</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858480</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858481" accession="SRX3397853">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397853</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858481</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858481: EE2_10nM_7; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692037">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692037</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858481</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858481</ID>
          <LABEL>GSM2858481</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858481</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858482" accession="SRX3397854">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397854</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858482</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858482: Mix_10nM_7; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692038">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692038</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858482</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858482</ID>
          <LABEL>GSM2858482</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858482</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858483" accession="SRX3397855">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397855</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858483</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858483: DMSO_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692039">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692039</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858483</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858483</ID>
          <LABEL>GSM2858483</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858483</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858484" accession="SRX3397856">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397856</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858484</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858484: BaP_10nM_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692040">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692040</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858484</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858484</ID>
          <LABEL>GSM2858484</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858484</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858485" accession="SRX3397857">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397857</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858485</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858485: EE2_10nM_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692041">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692041</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858485</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858485</ID>
          <LABEL>GSM2858485</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858485</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858486" accession="SRX3397858">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397858</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858486</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858486: EE2_1μM_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692042">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692042</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858486</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858486</ID>
          <LABEL>GSM2858486</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858486</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858487" accession="SRX3397859">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397859</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858487</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858487: Mix_10nM_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692043">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692043</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858487</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858487</ID>
          <LABEL>GSM2858487</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858487</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2858488" accession="SRX3397860">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3397860</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2858488</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2858488: Mix_1μM_8; Gadus morhua; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125080" refname="GSE106968">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125080</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2692044">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2692044</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2858488</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNA was isolated from frozen slices using mirVana™ miRNA Isolation Kit (Cat# AM1560, Ambion, Austin, TX, USA). The RNA was treated using TURBO DNase (TURBO DNA-free kit, Ambion) and further purified using RNA Clean &amp; Concentrator-5 (Zymo Research Corp, Irvine, CA, USA) and eluted with RNase-free water. The concentration of total RNA was measured using NanoDrop ND-1000 spectrophotometer (NanoDrop Technologies, Wilmington, DE, USA).  RNA quality was assessed using the Agilent 2100 bioanalyzer (Agilent Technologies, Palo Alto, CA). RNA samples (0.4 μg total RNA per sample) were sequenced according to Illumina TruSeq® Stranded mRNA Sample Preparation Guide on Illumina HiSeq 4000 (Illumina, Inc., San Diego, CA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302858488</ID>
          <LABEL>GSM2858488</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2858488</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
