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      <EXTERNAL_ID namespace="BioSample">SAMEA2475638</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>enok[1]_ovaries_3</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>7227</TAXON_ID>
      <SCIENTIFIC_NAME>Drosophila melanogaster</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Drosophila melanogaster was bred at Stowers Institute. The enok1 and enok2 mutant alleles originated from Bloomington Stock Center. Flies were grown on standard media at 25C unless stated otherwise. Larvae were heat shocked twice at 37C for 40 min, with 30 min break at 25C in between, for two consecutive days starting from the second day after hatching. Females were conditioned with wet yeast for 2-3 days before ovary dissection. Total RNA was isolated by Trizol, followed by DNase treatment. Libraries were poly-A selected and generated using the default directional Illumina protocol, TruSeq Adapters.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2014-10-22T17:01:00Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-08T17:28:46Z</VALUE>
      </SAMPLE_ATTRIBUTE>
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        <VALUE>2014-10-22T17:01:00Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>E-MTAB-2521:enok[1]_ovaries_3</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
        <VALUE>4-6 day</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>developmental stage</TAG>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>EMS induced mutation</VALUE>
      </SAMPLE_ATTRIBUTE>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>organism part</TAG>
        <VALUE>stages 5-14 egg chambers</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
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        <VALUE>E-MTAB-2521:enok[1]_ovaries_3</VALUE>
      </SAMPLE_ATTRIBUTE>
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  </SAMPLE>
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      <PRIMARY_ID>ERS445017</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA2475639</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>enok[1]_ovaries_2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>7227</TAXON_ID>
      <SCIENTIFIC_NAME>Drosophila melanogaster</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Drosophila melanogaster was bred at Stowers Institute. The enok1 and enok2 mutant alleles originated from Bloomington Stock Center. Flies were grown on standard media at 25C unless stated otherwise. Larvae were heat shocked twice at 37C for 40 min, with 30 min break at 25C in between, for two consecutive days starting from the second day after hatching. Females were conditioned with wet yeast for 2-3 days before ovary dissection. Total RNA was isolated by Trizol, followed by DNase treatment. Libraries were poly-A selected and generated using the default directional Illumina protocol, TruSeq Adapters.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
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      </SAMPLE_ATTRIBUTE>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>organism part</TAG>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
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        <VALUE>yw/+</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA2475640" accession="ERS445018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS445018</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA2475640</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>enok[2]_ovaries_2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>7227</TAXON_ID>
      <SCIENTIFIC_NAME>Drosophila melanogaster</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Drosophila melanogaster was bred at Stowers Institute. The enok1 and enok2 mutant alleles originated from Bloomington Stock Center. Flies were grown on standard media at 25C unless stated otherwise. Larvae were heat shocked twice at 37C for 40 min, with 30 min break at 25C in between, for two consecutive days starting from the second day after hatching. Females were conditioned with wet yeast for 2-3 days before ovary dissection. Total RNA was isolated by Trizol, followed by DNase treatment. Libraries were poly-A selected and generated using the default directional Illumina protocol, TruSeq Adapters.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2014-10-22T17:01:00Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2018-03-08T17:28:46Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
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        <VALUE>2014-10-22T17:01:00Z</VALUE>
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      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
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        <VALUE>4-6 day</VALUE>
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      </SAMPLE_ATTRIBUTE>
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        <VALUE>hs-Flp / +; FRTG13, enok[2] / FRTG13, ovo[D1-18]</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>organism part</TAG>
        <VALUE>stages 5-14 egg chambers</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
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  </SAMPLE>
</SAMPLE_SET>
