<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX6380680" alias="Phumanus_male_Illumina">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Phumanus_male_Illumina</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Phumanus_adult_male_Illumina</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Adults were sexed and pooled. 1 g of RNA was used to construct this library using the NEBNext kit and Oligos.  Libraries were quantified with NEBNext Quant Kit and sequenced using 150 bp paired-end reads on an Illumina HiSeq4000 machine.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041229">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041229</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Phumanus_Male</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Phumanus_male_Illumina</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6380681" alias="Phumanus_female_Illumina">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Phumanus_female_Illumina</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Phumanus_adult_female_Illumina</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Adults were sexed and pooled. 1 g of RNA was used to construct this library using the NEBNext kit and Oligos.  Libraries were quantified with NEBNext Quant Kit and sequenced using 150 bp paired-end reads on an Illumina HiSeq4000 machine.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041230">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041230</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Phumanus_Female</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Phumanus_female_Illumina</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6380682" alias="Rprolixus_male_Illumina">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Rprolixus_male_Illumina</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rprolixus_male_gonad_Illumina</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>1 g of RNA was used to construct this library using the NEBNext kit and Oligos.  Libraries were quantified with NEBNext Quant Kit and sequenced using 150 bp paired-end reads on an Illumina HiSeq4000 machine.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041231">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041231</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Rprolixus_Male</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Rprolixus_male_Illumina</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6380683" alias="Rprolixus_fem_Illumina">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Rprolixus_fem_Illumina</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Rprolixus_female_gonad_Illumina</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>1 g of RNA was used to construct this library using the NEBNext kit and Oligos.  Libraries were quantified with NEBNext Quant Kit and sequenced using 150 bp paired-end reads on an Illumina HiSeq4000 machine.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041232">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041232</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Rprolixus_Female</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Rprolixus_fem_Illumina</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6380684" alias="Bgermanica_male_Isoseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Bgermanica_male_Isoseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bgermanica__adult_male_Isoseq</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We extracted RNA from reproductive organs (gonad and colleterial glands) and fat body of a seven day old virgin female and from reproductive organs (gonad, conglobate gland, accessory glands, and seminal vesicles) and fat body of two seven day old males for library preparation. Tissues were pooled in Trizol, and a separate RNA extraction was done for each sex. Clontech SMARTER PCR cDNA synthesis kit and PrimeSTAR GXL DNA polymerase were used for cDNA synthesis; a cDNA SMRTbell kit was then used to add sequencing adapters. The male and female libraries were run on separate SMRT cells on the PacBio Sequel instrument, and the PacBio SMRTLink software was used for downstream data processing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041233">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041233</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Bgermanica_Male</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Bgermanica_male_Isoseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <PACBIO_SMRT>
        <INSTRUMENT_MODEL>Sequel</INSTRUMENT_MODEL>
      </PACBIO_SMRT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX6380685" alias="Bgermanica_fem_Isoseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX6380685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5519198">Bgermanica_fem_Isoseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Bgermanica_adult_female_Isoseq</TITLE>
    <STUDY_REF accession="SRP212479">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP212479</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB5519198">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We extracted RNA from reproductive organs (gonad and colleterial glands) and fat body of a seven day old virgin female and from reproductive organs (gonad, conglobate gland, accessory glands, and seminal vesicles) and fat body of two seven day old males for library preparation. Tissues were pooled in Trizol, and a separate RNA extraction was done for each sex. Clontech SMARTER PCR cDNA synthesis kit and PrimeSTAR GXL DNA polymerase were used for cDNA synthesis; a cDNA SMRTbell kit was then used to add sequencing adapters. The male and female libraries were run on separate SMRT cells on the PacBio Sequel instrument, and the PacBio SMRTLink software was used for downstream data processing.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS5041234">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS5041234</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|jwexler">Bgermanica_Female</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Bgermanica_fem_Isoseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <PACBIO_SMRT>
        <INSTRUMENT_MODEL>Sequel</INSTRUMENT_MODEL>
      </PACBIO_SMRT>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
