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  <EXPERIMENT alias="GSM2871614" accession="SRX3436769">
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      <PRIMARY_ID>SRX3436769</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871614</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871614: P3pHEnd_EC; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727718">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727718</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871614</EXTERNAL_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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          <DB>gds</DB>
          <ID>302871614</ID>
          <LABEL>GSM2871614</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2871615" accession="SRX3436770">
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      <PRIMARY_ID>SRX3436770</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871615</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871615: P8_pHEnd_EC_basal; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727713">
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          <PRIMARY_ID>SRS2727713</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871615</EXTERNAL_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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
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    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
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          <DB>gds</DB>
          <ID>302871615</ID>
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        <TAG>GEO Accession</TAG>
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  <EXPERIMENT alias="GSM2871616" accession="SRX3436771">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436771</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871616</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871616: 203P1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727714">
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          <PRIMARY_ID>SRS2727714</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
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          <DB>gds</DB>
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  <EXPERIMENT alias="GSM2871617" accession="SRX3436772">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436772</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871617</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871617: 32P1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727715">
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          <PRIMARY_ID>SRS2727715</PRIMARY_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
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    <EXPERIMENT_LINKS>
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        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871617</ID>
          <LABEL>GSM2871617</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871617</VALUE>
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  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871618" accession="SRX3436773">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436773</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871618</SUBMITTER_ID>
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    <TITLE>GSM2871618: 346P1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
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      <SAMPLE_DESCRIPTOR accession="SRS2727716">
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          <PRIMARY_ID>SRS2727716</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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
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    <EXPERIMENT_LINKS>
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          <DB>gds</DB>
          <ID>302871618</ID>
          <LABEL>GSM2871618</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871618</VALUE>
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  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871619" accession="SRX3436774">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436774</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871619</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871619: 347P1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125959" refname="GSE107574">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125959</PRIMARY_ID>
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      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727717">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727717</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871619</EXTERNAL_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>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Endoneurial microvessels were fluorescently detected in 20 micron thick axial cryosections of human sural nerve biopsies using UEA-1-FITC, and laser capture microdissection performed. Microvessels were stored in extraction buffer at -80oC and RNA isolated using Arcturus Pico Pure Isolation Kit (Thermo Fisher Scientific) or miRNeasy kit (Qiagen, Hilden, Germany). On-column DNase digestion was also performed to remove contaminating genomic DNA using the RNase-free DNase Set (Qiagen). cDNA libraries were generated using the SMARTer Stranded Total RNA-Seq Kit - Pico Input Mammalian (Clontech) and ribosomal cDNA was depleted prior to the final amplification step</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871619</ID>
          <LABEL>GSM2871619</LABEL>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871619</VALUE>
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</EXPERIMENT_SET>
