<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18249974" alias="GSM6730055_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249974</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730055_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730055: Whole muscle (TA), DEN, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744668">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744668</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730055</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730055</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249975" alias="GSM6730056_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249975</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730056_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730056: Whole muscle (TA), DEN, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744669">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744669</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730056</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730056</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249976" alias="GSM6730057_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249976</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730057_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730057: Whole muscle (TA), DEN, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744670">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744670</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730057</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730057</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249977" alias="GSM6730058_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249977</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730058_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730058: Whole muscle (TA), DEN, rep 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744671">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744671</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730058</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730058</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249978" alias="GSM6730059_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249978</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730059_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730059: Whole muscle (TA), sham, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744672">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744672</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730059</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730059</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249979" alias="GSM6730060_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249979</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730060_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730060: Whole muscle (TA), sham, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744673">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744673</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730060</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730060</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249980" alias="GSM6730061_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249980</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730061_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730061: Whole muscle (TA), sham, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744674">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744674</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730061</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730061</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249981" alias="GSM6730062_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249981</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730062_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730062: Whole muscle (TA), sham, rep 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744675">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744675</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730062</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730062</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249982" alias="GSM6730063_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249982</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730063_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730063: Muscle fibers (EDL), DEN, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744676">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744676</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730063</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730063</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249983" alias="GSM6730064_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249983</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730064_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730064: Muscle fibers (EDL), DEN, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744677">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744677</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730064</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730064</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249984" alias="GSM6730065_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249984</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730065_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730065: Muscle fibers (EDL), DEN, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744678">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744678</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730065</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730065</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249985" alias="GSM6730066_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249985</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730066_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730066: Muscle fibers (EDL), DEN, rep 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744679">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744679</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730066</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730066</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249986" alias="GSM6730067_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249986</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730067_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730067: Muscle fibers (EDL), sham, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744680">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744680</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730067</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730067</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249987" alias="GSM6730068_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249987</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730068_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730068: Muscle fibers (EDL), sham, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744681">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744681</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730068</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730068</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249988" alias="GSM6730069_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249988</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730069_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730069: Muscle fibers (EDL), sham, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744682">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744682</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730069</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730069</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18249989" alias="GSM6730070_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18249989</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6730070_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6730070: Muscle fibers (EDL), sham, rep 4; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP407779">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP407779</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA901417</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15744683">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15744683</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6730070</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6730070</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>TA muscles or EDL myofibers were homogenized in TRIzol reagent and RNA was isolated according to the manufacturer`s protocol (VWR, 30-2010) Library preparation was performed using the NEBNext Ultra II directional RNA kit with polyA molecule selection and unique dual indexing.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina NovaSeq 6000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
