<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17403214" alias="GSM6538008_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17403214</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6538008_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6538008: Blood, Naïve 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP395348">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395348</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE212586</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14961185">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14961185</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6538008</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6538008</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Blood mRNA was isolated using the Mouse Blood Ribopure RNA kit (Invitrogen).  Samples were treated with DNAse and Globinclear to remove genomic DNA and globin transcripts.  Quality of mRNA was asssessed by Ribolyzer Amplification and labeling of RNA samples were performed by the CBER/FDA Sequencing Core Facility using Illumina TotalPrep RNA Amplification (Applied Biosystems) and using an input of 1 mg of total RNA per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17403218" alias="GSM6538012_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17403218</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6538012_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6538012: Blood, BCG 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP395348">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395348</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE212586</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14961189">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14961189</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6538012</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6538012</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Blood mRNA was isolated using the Mouse Blood Ribopure RNA kit (Invitrogen).  Samples were treated with DNAse and Globinclear to remove genomic DNA and globin transcripts.  Quality of mRNA was asssessed by Ribolyzer Amplification and labeling of RNA samples were performed by the CBER/FDA Sequencing Core Facility using Illumina TotalPrep RNA Amplification (Applied Biosystems) and using an input of 1 mg of total RNA per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17403219" alias="GSM6538013_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17403219</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6538013_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6538013: Blood, BCG 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP395348">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP395348</PRIMARY_ID>
        <EXTERNAL_ID namespace="GEO">GSE212586</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS14961190">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS14961190</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6538013</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6538013</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Blood mRNA was isolated using the Mouse Blood Ribopure RNA kit (Invitrogen).  Samples were treated with DNAse and Globinclear to remove genomic DNA and globin transcripts.  Quality of mRNA was asssessed by Ribolyzer Amplification and labeling of RNA samples were performed by the CBER/FDA Sequencing Core Facility using Illumina TotalPrep RNA Amplification (Applied Biosystems) and using an input of 1 mg of total RNA per sample.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
