<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2197455" accession="SRX1837304">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1837304</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2197455</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2197455: piwi-ctrl; Drosophila melanogaster; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP076401" refname="GSE83236">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP076401</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1496699">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1496699</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2197455</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNAs (18-30nt) were isolated from ovaries by manual anion exchange chromatography procedure. Extracted small RNAs were cloned by BGI (China) for white-embKD_rep2 and piwi-embKD_rep2 and by Donnelly sequencing center (Canada) for piwi-ctrl, white-embKD and Piwi-emb-KD after being selected on acrylamide gel between 18 and 30 nucleotides.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302197455</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2197455</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2197456" accession="SRX1837305">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1837305</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2197456</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2197456: white-embKD; Drosophila melanogaster; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP076401" refname="GSE83236">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP076401</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1496703">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1496703</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2197456</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNAs (18-30nt) were isolated from ovaries by manual anion exchange chromatography procedure. Extracted small RNAs were cloned by BGI (China) for white-embKD_rep2 and piwi-embKD_rep2 and by Donnelly sequencing center (Canada) for piwi-ctrl, white-embKD and Piwi-emb-KD after being selected on acrylamide gel between 18 and 30 nucleotides.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302197456</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2197456</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2197457" accession="SRX1837306">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1837306</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2197457</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2197457: piwi-embKD; Drosophila melanogaster; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP076401" refname="GSE83236">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP076401</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1496701">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1496701</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2197457</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNAs (18-30nt) were isolated from ovaries by manual anion exchange chromatography procedure. Extracted small RNAs were cloned by BGI (China) for white-embKD_rep2 and piwi-embKD_rep2 and by Donnelly sequencing center (Canada) for piwi-ctrl, white-embKD and Piwi-emb-KD after being selected on acrylamide gel between 18 and 30 nucleotides.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302197457</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2197457</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2197458" accession="SRX1837307">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1837307</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2197458</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2197458: white-embKD_rep2; Drosophila melanogaster; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP076401" refname="GSE83236">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP076401</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1496700">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1496700</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2197458</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNAs (18-30nt) were isolated from ovaries by manual anion exchange chromatography procedure. Extracted small RNAs were cloned by BGI (China) for white-embKD_rep2 and piwi-embKD_rep2 and by Donnelly sequencing center (Canada) for piwi-ctrl, white-embKD and Piwi-emb-KD after being selected on acrylamide gel between 18 and 30 nucleotides.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302197458</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2197458</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2197459" accession="SRX1837308">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1837308</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2197459</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2197459: piwi-embKD_rep2; Drosophila melanogaster; ncRNA-Seq</TITLE>
    <STUDY_REF accession="SRP076401" refname="GSE83236">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP076401</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1496702">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1496702</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2197459</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>ncRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Small RNAs (18-30nt) were isolated from ovaries by manual anion exchange chromatography procedure. Extracted small RNAs were cloned by BGI (China) for white-embKD_rep2 and piwi-embKD_rep2 and by Donnelly sequencing center (Canada) for piwi-ctrl, white-embKD and Piwi-emb-KD after being selected on acrylamide gel between 18 and 30 nucleotides.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302197459</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2197459</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
