<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3242631" alias="Insect">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3242631</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3103530">Insect</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>First transcriptome analysis of an egg parasitoid Trichogramma chilonis</TITLE>
    <STUDY_REF accession="SRP119390">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP119390</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA412985</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Library preparation was performed at Genotypic Technology’s Genomics facility following Illumina TruSeq RNA library protocol outlined in “TruSeq RNA Sample Preparation Guide” ( Part # 15026495 Rev. F ). 1ug of Total RNA was subjected to Poly A purification of mRNA. Purified mRNA was fragmented for 3 minutes at elevated temperature (94 o C) in the presence of divalent cations and reverse transcribed with Superscript III Reverse transcriptase by priming with Random Hexamers. Second strand cDNA was synthesized in the presence of DNA Polymerase I and RnaseH. The cDNA was cleaned up using HighPrep PCR (MAGBIO, Cat# AC-60050). Illumina Adapters were ligated to the cDNA molecules after end repair and addition of A base. SPRI cleanup was performed after ligation. The library was amplified using 8 cycles of PCR for enrichment of adapter ligated fragments. The prepared library was quantified using Qubit and validated for quality by running an aliquot on High Sensitivity Bioanalyzer Chip (Agilent).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2565622">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2565622</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN07734740</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Insect</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
