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    </IDENTIFIERS>
    <TITLE>GSM1267495: Rev-Illumina; Drosophila melanogaster; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP033102</PRIMARY_ID>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For samples 1 &amp; 2, total RNA were extracted from 20 ovaries following provider procedure for the RNAqueous kit (Ambion) and 5 µgr were treated by GATC  to obtain PolyA+ RNA devoided of tRNA and rRNA. For samples 3 to 5,  we extracted polyA+ each from full bodies from 10 adult males (&lt;24 hour) and 10 adult females (0-3 days), and sequenced using Illumina HiSeq technology after random primed retrotranscription. Libraries were constructed using standard454 and Illumina instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX378809</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1267496</SUBMITTER_ID>
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    <TITLE>GSM1267496: IR6-Illumina; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP033102" refname="GSE52472">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP033102</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>For samples 1 &amp; 2, total RNA were extracted from 20 ovaries following provider procedure for the RNAqueous kit (Ambion) and 5 µgr were treated by GATC  to obtain PolyA+ RNA devoided of tRNA and rRNA. For samples 3 to 5,  we extracted polyA+ each from full bodies from 10 adult males (&lt;24 hour) and 10 adult females (0-3 days), and sequenced using Illumina HiSeq technology after random primed retrotranscription. Libraries were constructed using standard454 and Illumina instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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        <URL_LINK>
          <LABEL>GEO Sample GSM1267496</LABEL>
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  <EXPERIMENT alias="GSM1267497" accession="SRX378810" center_name="GEO">
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      <PRIMARY_ID>SRX378810</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1267497</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1267497: Iso1a-Illumina; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP033102" refname="GSE52472">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP033102</PRIMARY_ID>
        <SUBMITTER_ID namespace="GEO">GSE52472</SUBMITTER_ID>
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          <PRIMARY_ID>SRS503385</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1267497</EXTERNAL_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>For samples 1 &amp; 2, total RNA were extracted from 20 ovaries following provider procedure for the RNAqueous kit (Ambion) and 5 µgr were treated by GATC  to obtain PolyA+ RNA devoided of tRNA and rRNA. For samples 3 to 5,  we extracted polyA+ each from full bodies from 10 adult males (&lt;24 hour) and 10 adult females (0-3 days), and sequenced using Illumina HiSeq technology after random primed retrotranscription. Libraries were constructed using standard454 and Illumina instructions.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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          <LABEL>GEO Sample GSM1267497</LABEL>
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          <DB>gds</DB>
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