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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
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      <PRIMARY_ID>SRX5101439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
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      </IDENTIFIERS>
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    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111701</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY20</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>RBY20</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX5101440" alias="RBY22">
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      <PRIMARY_ID>SRX5101440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY22</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111702</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY22</SUBMITTER_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY22</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX5101441" alias="RBY9">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY9</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111703">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111703</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY9</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY9</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101442" alias="RBY8">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111704">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111704</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY8</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY8</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
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  <EXPERIMENT accession="SRX5101443" alias="RBY4">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111705">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111705</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY4</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101444" alias="RBY3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111706">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111706</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101445" alias="RBY2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111707">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111707</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101446" alias="RBY7">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111708">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111708</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY7</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY7</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101447" alias="RBY5">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111709</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY5</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY5</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101448" alias="RBY1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111710">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111710</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101449" alias="RBY18">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY18</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111711">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111711</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY18</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY18</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101450" alias="RBY17">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111712">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111712</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY17</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY17</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101451" alias="RBY21">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY21</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111713">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111713</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY21</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY21</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101452" alias="RBY15">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111714">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111714</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY15</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY15</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101453" alias="RBY13">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111715">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111715</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY13</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY13</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101454" alias="RBY19">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111716">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111716</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY19</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY19</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101455" alias="RBY23">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY23</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111717">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111717</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY23</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY23</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101456" alias="RBY11">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101456</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY11</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111718">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111718</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY11</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY11</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101457" alias="RBY10">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101457</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY10</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111719">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111719</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY10</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY10</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101458" alias="RBY6">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101458</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111720">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111720</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY6</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY6</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX5101459" alias="RBY16">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5101459</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4881760">RBY16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of homo sapiens: oocyte</TITLE>
    <STUDY_REF accession="SRP172762">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP172762</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4881760">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>From each single oocyte, cDNA was synthesized using SMART-Seq v4 ultra low input RNA kit (Clontech, cat # 634889).  Samples with RIN  9 were retained for library preparation.  An mRNA-seq library was then prepared from each sample using standard Illumina TruSeq protocol.  All libraries were multiplexed and sequenced on the same flow cell in order to minimize sequencing batch effect.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS4111721">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4111721</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|smithth">RBY16</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>RBY16</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
