<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17771502" alias="GSM6612968_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771502</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612968_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612968: NTB-24 [RSA.0000107295]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15297995">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15297995</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612968</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771503" alias="GSM6612969_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771503</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612969_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612969: NTB-37 [RSA.0000107296]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15297996">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15297996</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612969</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771504" alias="GSM6612970_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771504</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612970_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612970: NTB-38 [RSA.0000107297]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15297997">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15297997</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612970</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771505" alias="GSM6612971_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771505</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612971_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612971: NTB-40 [RSA.0000107298]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15297998">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15297998</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612971</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771506" alias="GSM6612972_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771506</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612972_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612972: NTB-42 [RSA.0000107299]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15297999">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15297999</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612972</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612972</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771507" alias="GSM6612973_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771507</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612973_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612973: NTB-44 [RSA.0000107300]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298000">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298000</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612973</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612973</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771508" alias="GSM6612974_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771508</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612974_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612974: NTB-50 [RSA.0000107301]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298001">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298001</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612974</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612974</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771509" alias="GSM6612975_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771509</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612975_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612975: NTB-57 [RSA.0000107302]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298002">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298002</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612975</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612975</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771510" alias="GSM6612976_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771510</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612976_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612976: TOV21g-IgG-18 [RSA.0000107303]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298003">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298003</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612976</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612976</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771511" alias="GSM6612977_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771511</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612977_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612977: TOV21g-IgG-19 [RSA.0000107304]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298004">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298004</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612977</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612977</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771512" alias="GSM6612978_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771512</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612978_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612978: TOV21g-IgG-25 [RSA.0000107305]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298005">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298005</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612978</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612978</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771513" alias="GSM6612979_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771513</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612979_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612979: TOV21g-IgG-26 [RSA.0000107306]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298006">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298006</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612979</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612979</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771514" alias="GSM6612980_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771514</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612980_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612980: TOV21g-IgG-28 [RSA.0000107307]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298007">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298007</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612980</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612980</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771515" alias="GSM6612981_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771515</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612981_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612981: TOV21g-IgG-31 [RSA.0000107308]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298008">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298008</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612981</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612981</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771516" alias="GSM6612982_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771516</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612982_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612982: TOV21g-IgG-47 [RSA.0000107309]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298009">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298009</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612982</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612982</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771517" alias="GSM6612983_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771517</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612983_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612983: TOV21g-IgG-52 [RSA.0000107310]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298010">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298010</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612983</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612983</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771518" alias="GSM6612984_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771518</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612984_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612984: TOV21g-mAB2-21 [RSA.0000107311]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298011">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298011</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612984</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612984</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771519" alias="GSM6612985_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771519</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612985_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612985: TOV21g-mAB2-46 [RSA.0000107312]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612985</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612985</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771520" alias="GSM6612986_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771520</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612986_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612986: TOV21g-mAB2-49 [RSA.0000107313]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612986</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612986</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771521" alias="GSM6612987_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771521</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612987_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612987: TOV21g-mAB2-55 [RSA.0000107314]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612987</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612987</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771522" alias="GSM6612988_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771522</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612988_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612988: NTB-58 [RSA.0000107275]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612988</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612988</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771523" alias="GSM6612989_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771523</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612989_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612989: NTB-59 [RSA.0000107276]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612989</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612989</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771524" alias="GSM6612990_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771524</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612990_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612990: NTB-78 [RSA.0000107277]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612990</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612990</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771525" alias="GSM6612991_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771525</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612991_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612991: NTB-82 [RSA.0000107278]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612991</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612991</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771526" alias="GSM6612992_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771526</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612992_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612992: NTB-87 [RSA.0000107279]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298019">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298019</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612992</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612992</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771527" alias="GSM6612993_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771527</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612993_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612993: NTB-88 [RSA.0000107280]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298020">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298020</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612993</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612993</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771528" alias="GSM6612994_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771528</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612994_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612994: TOV21g-IgG-8 [RSA.0000107281]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298021">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298021</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612994</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612994</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771529" alias="GSM6612995_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771529</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612995_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612995: TOV21g-IgG-10 [RSA.0000107282]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298022">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298022</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612995</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612995</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771530" alias="GSM6612996_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771530</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612996_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612996: TOV21g-IgG-64 [RSA.0000107283]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298023">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298023</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612996</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612996</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771531" alias="GSM6612997_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771531</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612997_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612997: TOV21g-IgG-65 [RSA.0000107284]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298024">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298024</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612997</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612997</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771532" alias="GSM6612998_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771532</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612998_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612998: TOV21g-IgG-75 [RSA.0000107285]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298025">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298025</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612998</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612998</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771533" alias="GSM6612999_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771533</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6612999_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6612999: TOV21g-IgG-84 [RSA.0000107286]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298026">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298026</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6612999</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6612999</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771534" alias="GSM6613000_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771534</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613000_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613000: TOV21g-mAB2-9 [RSA.0000107287]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298027">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298027</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613000</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613000</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771535" alias="GSM6613001_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771535</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613001_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613001: TOV21g-mAB2-16 [RSA.0000107288]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298028">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298028</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613001</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613001</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771536" alias="GSM6613002_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771536</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613002_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613002: TOV21g-mAB2-20 [RSA.0000107290]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298029">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298029</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613002</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613002</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771537" alias="GSM6613003_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771537</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613003_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613003: TOV21g-mAB2-56 [RSA.0000107291]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298030">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298030</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613003</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613003</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771538" alias="GSM6613004_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771538</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613004_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613004: TOV21g-mAB2-62 [RSA.0000107292]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298031">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298031</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613004</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613004</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771539" alias="GSM6613005_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771539</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613005_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613005: TOV21g-mAB2-63 [RSA.0000107293]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298032">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298032</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613005</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613005</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17771540" alias="GSM6613006_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17771540</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6613006_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6613006: TOV21g-mAB2-77 [RSA.0000107294]; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP400565">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP400565</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA886080</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15298033">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15298033</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6613006</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6613006</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted and purified with QIAzol lysis reagent and RNeasy kits (Qiagen Inc., Germantown, MD, USA) from snap-frozen muscle tissues. 1ug of total RNA was used for library construction. RNA was converted into sequencing libraries using an Illumina TruSeq Stranded mRNA library prep kit (Illumina, San Diego, CA, USA) with Sciclone G3 NGSx workstation (PerkinElmer, Waltham, MA, USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
