<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="rAFI" accession="SRX1557580">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557580</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAFI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate female: Sample Znev_rAF1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272914">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272914</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAFI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
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          <SPOT_LENGTH>302</SPOT_LENGTH>
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            <READ_INDEX>0</READ_INDEX>
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            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rAFII" accession="SRX1557581">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557581</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAFII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate female: Sample Znev_rAF2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272913">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272913</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAFII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
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          <PAIRED/>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</SPOT_LENGTH>
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            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rAFIII" accession="SRX1557582">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557582</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAFIII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate female: Sample Znev_rAF3</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272912">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272912</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAFIII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rAMI" accession="SRX1557583">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557583</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAMI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate male: Sample Znev_rAM1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272911">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272911</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAMI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rAMII" accession="SRX1557584">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557584</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAMII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate male: Sample Znev_rAM2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272910">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272910</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAMII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rAMIII" accession="SRX1557585">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557585</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rAMIII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: alate male: Sample Znev_rAM3</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272909">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272909</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rAMIII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rWFI" accession="SRX1557586">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557586</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWFI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker female: Sample Znev_rWF1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272908">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272908</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWFI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rWFII" accession="SRX1557587">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557587</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWFII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker female: Sample Znev_rWF2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272907">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272907</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWFII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rWFIII" accession="SRX1557588">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557588</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWFIII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker female: Sample Znev_rWF3</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272906">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272906</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWFIII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1557589" alias="rWMI">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557589</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWMI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker male: Sample Znev_rWM1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA309979</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272905">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272905</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04443357</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWMI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>300</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>151</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX1557590" alias="rWMII">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557590</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWMII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker male: Sample Znev_rWM2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA309979</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272904">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272904</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN04443358</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWMII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>300</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>151</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="rWMIII" accession="SRX1557591">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557591</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">rWMIII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-Seq of Zootermopsis nevadensis: worker male: Sample Znev_rWM3</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Total RNA was extracted from single individual termites in 1ml of Trizol(R) Reagent (Life Technologies) according to manufacturer's instructions.  The extracted RNA was suspended in 40 uL Nuclease Free Water (Ambion) and was treated with TURBO DNA-free(TM) kit (Ambion) to remove the genomic DNA contamination.  RNA concentration was measured by Qubit(R) 2.0 fluorometer (Life Technologies, Carlsbad) and RNA integrity was checked by Agilent RNA 600 nano kit (Bioanalyzer, Agilent Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272903">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272903</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>rWMIII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dAFI" accession="SRX1557592">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557592</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dAFI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: alate female: Sample Znev_dAF1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272902">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272902</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dAFI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dAFII" accession="SRX1557593">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557593</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dAFII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: alate female: Sample Znev_dAF2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272901">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272901</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dAFII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dAMI" accession="SRX1557594">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557594</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dAMI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: alate male: Sample Znev_dAM1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272900">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272900</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dAMI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dAMII" accession="SRX1557595">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557595</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dAMII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: alate male: Sample Znev_dAM2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272899">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272899</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dAMII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dWFI" accession="SRX1557596">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557596</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dWFI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: worker female: Sample Znev_dWF1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272898">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272898</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dWFI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dWFII" accession="SRX1557597">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557597</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dWFII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: worker female: Sample Znev_dWF2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272897">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272897</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dWFII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dWMI" accession="SRX1557598">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557598</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dWMI</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: worker male: Sample Znev_dWM1</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272896">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272896</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dWMI</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="dWMII" accession="SRX1557599">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1557599</PRIMARY_ID>
      <SUBMITTER_ID namespace="Georgia Institute of Technology">dWMII</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bisulfite-Seq of Zootermopsis nevadensis: worker male: Sample Znev_dWM2</TITLE>
    <STUDY_REF accession="SRP069201">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP069201</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>"Genomic DNA was isolated from a pool of five individual termites (except for male alates where only four individuals were used) using MasterPure(TM) Complete DNA and RNA Purification Kit (Epicentre) according to manufacturer's protocol. The extracted DNA was suspended in 35uL TE buffer.  DNA concentration was determined by Qubit(R) 2.0 fluorometer (Life Technologies). Bisulfite converted DNA and mRNA library preparation was performed in Georgia (http://dna.uga.edu), and sequencing was performed using the Illumina NextSeq500 platform."</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1272895">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1272895</PRIMARY_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>dWMII</LIBRARY_NAME>
        <LIBRARY_STRATEGY>Bisulfite-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>302</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>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>152</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
