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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4509808" alias="LC 15-3">
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      <PRIMARY_ID>SRX4509808</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">LC 15-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum Low CO2 3</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3629290">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629290</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LC 15-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4509809" alias="LC 15-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4509809</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">LC 15-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum Low CO2 2</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629289</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LC 15-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX4509810</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">LC 15-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum Low CO2 1</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3629291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>LC 15-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4509811" alias="HC15-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4509811</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">HC15-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum high CO2 3</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3629292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HC15-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4509812" alias="HC15-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4509812</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">HC15-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum high CO2 2</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3629293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HC15-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4509813" alias="HC15-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4509813</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4368566">HC15-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ssRNA-seq Phaeodatylum tricornutum high CO2 1</TITLE>
    <STUDY_REF accession="SRP156408">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP156408</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA484278</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>A total amount of 3 g RNA per sample was used as initial material for the RNA sample preparations. Ribosomal RNA was removed using Epicentre Ribo-Zero Gold Kits(Human/Mouse/Rat)Epicentre, USA.Subsequently, the sequencing libraries were generated following manufacturer recommendations with varied index label by NEBNext Ultra Directional RNA Library Prep Kit for Illumina (NEB, Ispawich, USA) .</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3629294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3629294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN09762566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HC15-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
