<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM3553687" accession="SRX5222978">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222978</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553687</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553687: S1 DiabeticBMDM_unstimulated_rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553687</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553687</ID>
          <LABEL>GSM3553687</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553687</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553688" accession="SRX5222979">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222979</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553688</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553688: S2 DiabeticBMDM_unstimulated_rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553688</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553688</ID>
          <LABEL>GSM3553688</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553688</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553689" accession="SRX5222980">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222980</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553689</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553689: S3  ControlBMDM_unstimulated_rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553689</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553689</ID>
          <LABEL>GSM3553689</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553689</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553690" accession="SRX5222981">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222981</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553690</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553690: S4 ControlBMDM_unstimulated_rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553690</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553690</ID>
          <LABEL>GSM3553690</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553690</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553691" accession="SRX5222982">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222982</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553691</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553691: S5 DiabeticBMDM_unstimulated_rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553691</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553691</ID>
          <LABEL>GSM3553691</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553691</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553692" accession="SRX5222983">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222983</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553692</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553692: S6 DiabeticBMDM_unstimulated_rep4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553692</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553692</ID>
          <LABEL>GSM3553692</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553692</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553693" accession="SRX5222984">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222984</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553693</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553693: S7 ControlBMDM_unstimulated_rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553693</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553693</ID>
          <LABEL>GSM3553693</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553693</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553694" accession="SRX5222985">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222985</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553694</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553694: S8 ControlBMDM_unstimulated_rep4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553694</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553694</ID>
          <LABEL>GSM3553694</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553694</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553695" accession="SRX5222986">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222986</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553695</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553695: S9 DiabeticBMDM_unstimulated_rep5; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553695</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553695</ID>
          <LABEL>GSM3553695</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553695</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553696" accession="SRX5222987">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222987</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553696</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553696: S10 DiabeticBMDM_unstimulated_rep6; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553696</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553696</ID>
          <LABEL>GSM3553696</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553696</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553697" accession="SRX5222988">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222988</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553697</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553697: S11 ControlBMDM_unstimulated_rep5; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553697</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553697</ID>
          <LABEL>GSM3553697</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553697</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553698" accession="SRX5222989">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222989</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553698</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553698: S12 ControlBMDM_unstimulated_rep6; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553698</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553698</ID>
          <LABEL>GSM3553698</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553698</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553699" accession="SRX5222990">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222990</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553699</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553699: S13 DiabeticBMDM_LPSstimulated_rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553699</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553699</ID>
          <LABEL>GSM3553699</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553699</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553700" accession="SRX5222991">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222991</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553700</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553700: S14 DiabeticBMDM_LPSstimulated_rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553700</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553700</ID>
          <LABEL>GSM3553700</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553700</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553701" accession="SRX5222992">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222992</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553701</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553701: S15 ControlBMDM_LPSstimulated_rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553701</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553701</ID>
          <LABEL>GSM3553701</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553701</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553702" accession="SRX5222993">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222993</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553702</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553702: S16 ControlBMDM_LPSstimulated_rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553702</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553702</ID>
          <LABEL>GSM3553702</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553702</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553703" accession="SRX5222994">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222994</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553703</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553703: S17 DiabeticBMDM_LPSstimulated_rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553703</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553703</ID>
          <LABEL>GSM3553703</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553703</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553704" accession="SRX5222995">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222995</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553704</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553704: S18 DiabeticBMDM_LPSstimulated_rep4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553704</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553704</ID>
          <LABEL>GSM3553704</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553704</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553705" accession="SRX5222996">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222996</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553705</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553705: S19 ControlBMDM_LPSstimulated_rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227021">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227021</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553705</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553705</ID>
          <LABEL>GSM3553705</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553705</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553706" accession="SRX5222997">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222997</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553706</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553706: S20 ControlBMDM_LPSstimulated_rep4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227020">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227020</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553706</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553706</ID>
          <LABEL>GSM3553706</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553706</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553707" accession="SRX5222998">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222998</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553707</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553707: S21 DiabeticBMDM_LPSstimulated_rep5; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227022">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227022</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553707</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553707</ID>
          <LABEL>GSM3553707</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553707</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553708" accession="SRX5222999">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5222999</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553708</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553708: S22 DiabeticBMDM_LPSstimulated_rep6; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227023">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227023</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553708</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553708</ID>
          <LABEL>GSM3553708</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553708</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553709" accession="SRX5223000">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5223000</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553709</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553709: S23 ControlBMDM_LPSstimulated_rep5; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227024">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227024</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553709</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553709</ID>
          <LABEL>GSM3553709</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553709</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3553710" accession="SRX5223001">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5223001</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3553710</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3553710: S24 ControlBMDM_LPSstimulated_rep6; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP176486" refname="GSE124774">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP176486</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4227025">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4227025</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3553710</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and RNA isolated using mirVana mRNA/miRNA isolation kit (ThermoFisher Scientific, UK), according to manufacturer's instructions. RNA-seq libraries were prepared with the TruSeq Stranded mRNA LT sample preparation kit (Illumina, UK) using both Sciclone and Zephyr liquid handling robotics (PerkinElmer, UK). Library concentrations were quantified with the Qubit Fluoro-metric Quantitation system (Life Technologies, UK) and the size distribution was assessed using the Experion Automated Electrophoresis System (Bio-Rad, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 4000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303553710</ID>
          <LABEL>GSM3553710</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3553710</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
