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      <PRIMARY_ID>SRX22883429</PRIMARY_ID>
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    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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        <PRIMARY_ID>SRP477878</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2500</DESIGN_DESCRIPTION>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22883430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2501</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS19855772</PRIMARY_ID>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22883431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC4</SUBMITTER_ID>
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    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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        <PRIMARY_ID>SRP477878</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2510</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855773</PRIMARY_ID>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX22883432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2511</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855774</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow1</SUBMITTER_ID>
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        <LIBRARY_NAME>TL1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX22883433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2512</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855775</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh5</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>TH5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2513</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855776</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempControl6</SUBMITTER_ID>
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        <LIBRARY_NAME>TC6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2514</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855777</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow8</SUBMITTER_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2515</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855778</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh7</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2516</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855779</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempControl1</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2517</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855780</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow4</SUBMITTER_ID>
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        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2518</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855781</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TL2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2519</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855782</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TH8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2502</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855783</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TL5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2503</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19855784">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855784</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempControl5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TC5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2504</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855785</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow7</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TL7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2505</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855786</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TH1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2506</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855787</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TH3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TC7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2507</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855788</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempControl7</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TC7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TL3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2508</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855789</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempLow3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TL3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX22883448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB14053600">TH4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Crassostrea virginica: adult</TITLE>
    <STUDY_REF accession="SRP477878">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP477878</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB14053600">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole oysters were homogenized into RNAlater solution using a tissue homogenizer. RNA was isolated using Qiagen RNeasy mini kit using the manufacturers protocol and with an additional on column DNase I treatment. Concentration of RNA was assessed using nanodrop spectrophotometry and Bioanalyzer RNA 6000 nano kit. RNAseq was completed on each sampling using Illumina HiSeq 2509</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS19855790">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS19855790</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|stephanie.hall.0890@gmail.com">TempHigh4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>TH4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
