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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3443634" alias="mil1b-d3-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443634</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">mil1b-d3-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>mil1b-d3-4</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734252">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734252</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>mil1b-d3-4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443635" alias="mil1b-d3-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443635</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">mil1b-d3-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>mil1b-d3-3</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734251">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734251</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>mil1b-d3-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443636" alias="il1b-d3-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443636</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">il1b-d3-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>il1b-d3-2</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734254">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734254</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>il1b-d3-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="il1b-d3-1" accession="SRX3443637">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443637</PRIMARY_ID>
      <SUBMITTER_ID namespace="UC Davis">il1b-d3-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>il1b-d3-1</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734253">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734253</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>il1b-d3-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>286</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443638" alias="wt-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443638</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">wt-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>wt-2</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734255">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734255</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>wt-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443639" alias="wt-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443639</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">wt-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>wt-1</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734257">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734257</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>wt-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443640" alias="wt-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443640</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">wt-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>wt-4</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734256">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734256</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>wt-4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443641" alias="mwt-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443641</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">mwt-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>mwt-3</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734258">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734258</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>mwt-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443642" alias="il1b-2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443642</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">il1b-2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>il1b-2</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734259">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734259</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>il1b-2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443643" alias="il1b-1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443643</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">il1b-1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>il1b-1</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734260">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734260</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>il1b-1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443644" alias="mil1b-4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443644</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">mil1b-4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>mil1b-4</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734262">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734262</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>mil1b-4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3443645" alias="il1b-3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3443645</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3294404">il1b-3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>il1b-3</TITLE>
    <STUDY_REF accession="SRP126124">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP126124</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA421032</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Indexed libraries were constructed from 1000 ng of total RNA using the TruSeq Stranded mRNA Sample Prep Kit (Illumina) following the manufacturer's instruction. The quantity and quality of the libraries were also assessed by Qubit and Agilent 2100 Bioanalyzer, respectively. The average library size was 400 bp. Libraries molar concentration were validated by qPCR for library pooling.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2734261">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2734261</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN08130970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>il1b-3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>unspecified</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
