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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX12677169" alias="GSM5631527_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677169</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631527_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631527: evening control, non-sleep deprived EC3; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628739">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628739</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631527</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631527</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677168" alias="GSM5631526_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677168</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631526_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631526: evening control, non-sleep deprived EC2; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628742">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628742</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631526</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631526</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677167" alias="GSM5631525_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677167</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631525_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631525: evening control, non-sleep deprived EC1; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628738">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628738</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631525</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631525</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677170" alias="GSM5631528_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677170</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631528_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631528: evening sleep deprivation ESD1; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628741">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628741</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631528</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631528</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677171" alias="GSM5631529_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677171</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631529_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631529: evening sleep deprivation ESD2; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628740">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628740</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631529</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631529</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677172" alias="GSM5631530_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677172</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631530_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631530: evening sleep deprivation ESD3; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628743">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628743</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631530</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631530</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677174" alias="GSM5631532_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677174</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631532_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631532: morning control, non-sleep deprived MC2; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628745">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628745</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631532</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631532</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677175" alias="GSM5631533_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677175</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631533_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631533: morning control, non-sleep deprived MC3; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628746">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628746</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631533</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631533</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677173" alias="GSM5631531_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677173</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631531_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631531: morning control, non-sleep deprived MC1; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628744">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628744</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631531</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631531</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677177" alias="GSM5631535_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677177</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631535_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631535: morning sleep deprivation MSD2; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628747">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628747</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631535</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631535</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677178" alias="GSM5631536_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677178</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631536_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631536: morning sleep deprivation MSD3; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628748">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628748</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631536</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631536</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX12677176" alias="GSM5631534_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX12677176</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM5631534_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM5631534: morning sleep deprivation MSD1; Drosophila melanogaster; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP341965">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP341965</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE186076</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS10628749">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS10628749</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM5631534</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM5631534</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>40-45 Brains from 7-10 day old flies expressing gfp in ~15 R5 ellipsoid body neurons in morning or evening +/- sleep deprivation conditions were dissected. Flourescent-activated cell sorting (FACS) was used to isolate individual cells. Total RNA was extracted using PicoPure kit and cDNA was created using a T7-oligo-dT primer and SuperScript III and served as a template to make and amplify new mRNA using T7 RNA polymerase and the Ambion MegaScript kit . Libraries were generated using an Illumina TruSeq Stranded Kit</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
