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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX2036014</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;AutW132_replicate_1</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX2036016</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;OregonR_replicate_1</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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        <PRIMARY_ID>SRP082430</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX2036017</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;OregonR_replicate_1</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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        <PRIMARY_ID>SRP082430</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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          <SINGLE/>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX2036018</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;OregonR_replicate_2</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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        <PRIMARY_ID>SRP082430</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;OregonR_replicate_3</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;AutW132_replicate_1</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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          <SINGLE/>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;AutW132_replicate_2</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <SUBMITTER_ID namespace="SUB1782352">Female_OregonR;AutW132_replicate_3</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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      <SUBMITTER_ID namespace="SUB1782352">Female_SiI;OregonR_replicate_1</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <SUBMITTER_ID namespace="SUB1782352">Female_SiI;OregonR_replicate_2</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629908</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596145</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
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          <SINGLE/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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      <PRIMARY_ID>SRX2036025</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_OregonR;OregonR_replicate_2</SUBMITTER_ID>
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    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
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    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
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          <EXTERNAL_ID namespace="BioSample">SAMN05596128</EXTERNAL_ID>
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      <LIBRARY_DESCRIPTOR>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036026" alias="Female_SiI;OregonR_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036026</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Female_SiI;OregonR_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629910">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629910</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Female_SiI;OregonR_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036027" alias="Female_SiI;AutW132_replicate_1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036027</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Female_SiI;AutW132_replicate_1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629911">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629911</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Female_SiI;AutW132_replicate_1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036028" alias="Female_SiI;AutW132_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036028</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Female_SiI;AutW132_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629912">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629912</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Female_SiI;AutW132_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036029" alias="Male_SiI;AutW132_replicate_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036029</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;AutW132_replicate_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629913">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629913</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_SiI;AutW132_replicate_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036030" alias="Male_SiI;OregonR_replicate_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036030</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;OregonR_replicate_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629914">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629914</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_SiI;OregonR_replicate_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036031" alias="Male_OregonR;AutW132_replicate_2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036031</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_OregonR;AutW132_replicate_2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629915">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629915</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_OregonR;AutW132_replicate_2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036032" alias="Male_OregonR;OregonR_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036032</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_OregonR;OregonR_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629917">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629917</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_OregonR;OregonR_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036033" alias="Male_SiI;OregonR_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036033</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;OregonR_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629918">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629918</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_SiI;OregonR_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036034" alias="Male_OregonR;AutW132_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036034</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_OregonR;AutW132_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629916">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629916</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_OregonR;AutW132_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2036035" alias="Male_SiI;AutW132_replicate_3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2036035</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB1782352">Male_SiI;AutW132_replicate_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Mitonuclear transcriptomics in Drosophila</TITLE>
    <STUDY_REF accession="SRP082430">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP082430</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA339542</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>30 x 5 day old whole flies were used as tissue for RNA extraction. The work-flow was as follows: mRNA extracted -&gt; RNA fragmented -&gt; 1st then 2nd strand cDNA synthesis -&gt; End-IT end repair -&gt; Addition of 'A' bases -&gt; Adapter ligation (TruSeq)-&gt; PCR enrichment.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS1629919">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1629919</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN05596135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Male_SiI;AutW132_replicate_3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
