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    <TITLE>GSM1910282: NLN01; Homo sapiens; RNA-Seq</TITLE>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <TITLE>GSM1910283: NLN02; Homo sapiens; RNA-Seq</TITLE>
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      <PRIMARY_ID>SRX1341828</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910284</SUBMITTER_ID>
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    <TITLE>GSM1910284: NLN03; Homo sapiens; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
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          <DB>gds</DB>
          <ID>301910284</ID>
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      <PRIMARY_ID>SRX1341829</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910285</SUBMITTER_ID>
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    <TITLE>GSM1910285: NLN04; Homo sapiens; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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          <PRIMARY_ID>SRS1117382</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX1341830</PRIMARY_ID>
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    <TITLE>GSM1910286: NLN06; Homo sapiens; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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          <PRIMARY_ID>SRS1117381</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX1341831</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910287</SUBMITTER_ID>
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    <TITLE>GSM1910287: NLN07; Homo sapiens; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
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          <PRIMARY_ID>SRS1117380</PRIMARY_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
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        <TAG>GEO Accession</TAG>
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      <PRIMARY_ID>SRX1341832</PRIMARY_ID>
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    <TITLE>GSM1910288: NLN08; Homo sapiens; RNA-Seq</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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          <PRIMARY_ID>SRS1117379</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX1341833</PRIMARY_ID>
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    <TITLE>GSM1910289: NLN09; Homo sapiens; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX1341834</PRIMARY_ID>
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    <TITLE>GSM1910290: NLN10; Homo sapiens; RNA-Seq</TITLE>
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        <PRIMARY_ID>SRP064912</PRIMARY_ID>
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          <PRIMARY_ID>SRS1117377</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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      <PRIMARY_ID>SRX1341835</PRIMARY_ID>
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    <TITLE>GSM1910291: NLN12; Homo sapiens; RNA-Seq</TITLE>
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          <SINGLE/>
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        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341836</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910292</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910292: FL03; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117374">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117374</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910292</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910292</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910292</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910293" accession="SRX1341837">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341837</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910293: FL04; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117373">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117373</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910293</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910293</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910294" accession="SRX1341838">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341838</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910294: FL06; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117372">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117372</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910294</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910294</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910295" accession="SRX1341839">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341839</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910295</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910295: FL08; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117371">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117371</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910295</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910295</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910295</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910296" accession="SRX1341840">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341840</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910296</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910296: FL09; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117376">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117376</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910296</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910296</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910296</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910297" accession="SRX1341841">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341841</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910297: FL10; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117370">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117370</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910297</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910297</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910297</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910298" accession="SRX1341842">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341842</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910298: FL11; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117369">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117369</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910298</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910298</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910298</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910299" accession="SRX1341843">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341843</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910299: FL12; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117367">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117367</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910299</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910299</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910299</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910300" accession="SRX1341844">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341844</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910300: FL13; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117368">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117368</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910300</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910300</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910300</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910301" accession="SRX1341845">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341845</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910301: FL14; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117366">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117366</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910301</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910301</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910301</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910302" accession="SRX1341846">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341846</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910302: FL101; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117365">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117365</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910302</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910302</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910302</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910303" accession="SRX1341847">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341847</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910303: FL102; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117363">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117363</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910303</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910303</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910303</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910304" accession="SRX1341848">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341848</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910304: RLN01; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117364">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117364</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910304</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910304</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910304</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910305" accession="SRX1341849">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341849</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910305</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910305: RLN02; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117362">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117362</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910305</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910305</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910305</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910306" accession="SRX1341850">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341850</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910306: RLN03; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117361">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117361</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910306</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910306</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910306</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910307" accession="SRX1341851">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341851</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910307: RLN05; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117360">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117360</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910307</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910307</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910307</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1910308" accession="SRX1341852">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX1341852</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1910308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1910308: RLN07; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP064912" refname="GSE74102">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP064912</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS1117359">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS1117359</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1910308</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Regulatory T cells were sorted by FACS from single cell suspensions.  Total RNA was extracted using AllPrep DNA/RNA Micro Kit (Qiagen) following manufacturers protocol.  RNA quality was assessed by 2100 BioAnalyzer (Agilent). Total RNA was used for cDNA synthesis using Ovation RNA-Seq (NuGEN) with normalized RNA input for each sample.  Amplified cDNA was purified through MinElute reaction cleanup column (Qiagen).  cDNA quality was assessed using 2100 BioAnalyzer (Agilent).  SOLiD protocols were followed for library prepartion for 50bp sequencing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ABI_SOLID>
        <INSTRUMENT_MODEL>AB SOLiD 4 System</INSTRUMENT_MODEL>
      </ABI_SOLID>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301910308</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1910308</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
