<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18385149" alias="GSM6757104_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385149</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757104_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757104: Stool sRNA-Seq - Patient 10 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870763">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870763</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385150" alias="GSM6757105_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385150</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757105_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757105: Stool sRNA-Seq - Patient 10 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870764">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870764</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385151" alias="GSM6757106_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385151</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757106_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757106: Stool sRNA-Seq - Patient 10 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870765">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870765</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385152" alias="GSM6757107_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385152</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757107_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757107: Stool sRNA-Seq - Patient 11 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870766">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870766</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385153" alias="GSM6757108_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385153</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757108_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757108: Stool sRNA-Seq - Patient 11 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870767">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870767</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385154" alias="GSM6757109_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385154</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757109_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757109: Stool sRNA-Seq - Patient 11 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870768">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870768</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757109</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757109</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385155" alias="GSM6757110_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385155</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757110_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757110: Stool sRNA-Seq - Patient 13 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870769">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870769</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757110</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757110</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385156" alias="GSM6757111_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385156</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757111_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757111: Stool sRNA-Seq - Patient 13 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870770">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870770</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757111</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757111</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385157" alias="GSM6757112_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385157</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757112_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757112: Stool sRNA-Seq - Patient 13 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870771">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870771</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757112</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757112</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385158" alias="GSM6757113_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385158</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757113_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757113: Stool sRNA-Seq - Patient 14 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870772">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870772</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757113</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757113</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385159" alias="GSM6757114_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385159</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757114_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757114: Stool sRNA-Seq - Patient 14 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870773">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870773</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757114</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757114</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385160" alias="GSM6757115_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385160</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757115_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757115: Stool sRNA-Seq - Patient 14 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870774">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870774</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757115</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757115</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385161" alias="GSM6757116_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385161</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757116_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757116: Stool sRNA-Seq - Patient 15 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870775">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870775</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757116</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757116</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385162" alias="GSM6757117_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385162</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757117_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757117: Stool sRNA-Seq - Patient 15 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870776">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870776</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757117</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757117</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385163" alias="GSM6757118_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385163</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757118_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757118: Stool sRNA-Seq - Patient 15 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870777">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870777</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757118</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757118</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385164" alias="GSM6757119_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385164</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757119_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757119: Stool sRNA-Seq - Patient 17 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870778">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870778</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757119</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757119</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385165" alias="GSM6757120_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385165</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757120_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757120: Stool sRNA-Seq - Patient 17 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870779">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870779</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757120</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757120</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385166" alias="GSM6757121_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385166</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757121_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757121: Stool sRNA-Seq - Patient 17 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870780">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870780</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757121</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757121</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385167" alias="GSM6757122_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385167</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757122_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757122: Stool sRNA-Seq - Patient 18 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870781">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870781</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757122</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757122</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385168" alias="GSM6757123_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385168</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757123_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757123: Stool sRNA-Seq - Patient 18 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870782">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870782</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757123</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757123</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385169" alias="GSM6757124_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385169</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757124_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757124: Stool sRNA-Seq - Patient 18 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870783">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870783</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757124</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757124</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385170" alias="GSM6757125_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385170</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757125_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757125: Stool sRNA-Seq - Patient 19 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870784">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870784</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757125</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757125</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385171" alias="GSM6757126_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385171</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757126_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757126: Stool sRNA-Seq - Patient 19 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870785">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870785</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757126</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757126</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385172" alias="GSM6757127_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385172</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757127_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757127: Stool sRNA-Seq - Patient 19 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870786">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870786</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757127</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757127</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385173" alias="GSM6757128_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385173</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757128_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757128: Stool sRNA-Seq - Patient 20 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870787">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870787</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757128</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757128</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385174" alias="GSM6757129_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385174</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757129_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757129: Stool sRNA-Seq - Patient 20 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870788">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870788</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757129</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757129</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385175" alias="GSM6757130_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385175</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757130_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757130: Stool sRNA-Seq - Patient 20 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870789">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870789</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757130</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757130</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385176" alias="GSM6757131_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385176</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757131_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757131: Stool sRNA-Seq - Patient 21 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870790">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870790</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757131</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757131</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385177" alias="GSM6757132_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385177</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757132_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757132: Stool sRNA-Seq - Patient 21 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870791">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870791</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757132</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757132</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385178" alias="GSM6757133_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385178</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757133_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757133: Stool sRNA-Seq - Patient 21 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870792">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870792</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757133</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757133</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385179" alias="GSM6757134_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385179</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757134_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757134: Stool sRNA-Seq - Patient 22 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870793">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870793</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757134</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757134</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385180" alias="GSM6757135_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385180</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757135_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757135: Stool sRNA-Seq - Patient 22 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870794">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870794</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757135</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757135</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385181" alias="GSM6757136_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385181</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757136_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757136: Stool sRNA-Seq - Patient 22 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870795">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870795</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757136</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757136</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385182" alias="GSM6757137_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385182</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757137_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757137: Stool sRNA-Seq - Patient 23 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870796">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870796</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757137</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757137</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385183" alias="GSM6757138_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385183</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757138_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757138: Stool sRNA-Seq - Patient 23 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870797">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870797</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757138</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757138</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385184" alias="GSM6757139_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385184</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757139_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757139: Stool sRNA-Seq - Patient 23 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870798">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870798</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757139</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757139</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385185" alias="GSM6757140_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385185</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757140_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757140: Stool sRNA-Seq - Patient 24 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870799">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870799</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757140</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757140</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385186" alias="GSM6757141_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385186</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757141_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757141: Stool sRNA-Seq - Patient 24 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870800">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870800</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757141</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757141</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385187" alias="GSM6757142_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385187</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757142_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757142: Stool sRNA-Seq - Patient 24 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870801">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870801</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757142</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757142</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385188" alias="GSM6757143_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385188</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757143_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757143: Stool sRNA-Seq - Patient 25 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870802">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870802</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757143</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757143</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385189" alias="GSM6757144_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385189</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757144_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757144: Stool sRNA-Seq - Patient 25 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870803">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870803</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757144</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757144</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385190" alias="GSM6757145_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385190</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757145_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757145: Stool sRNA-Seq - Patient 25 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870804">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870804</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757145</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757145</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385191" alias="GSM6757146_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385191</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757146_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757146: Stool sRNA-Seq - Patient 26 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870805">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870805</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757146</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757146</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385192" alias="GSM6757147_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385192</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757147_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757147: Stool sRNA-Seq - Patient 26 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870806">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870806</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757147</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757147</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385193" alias="GSM6757148_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385193</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757148_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757148: Stool sRNA-Seq - Patient 26 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870807">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870807</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757148</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757148</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385194" alias="GSM6757149_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385194</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757149_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757149: Stool sRNA-Seq - Patient 28 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870808">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870808</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757149</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757149</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385195" alias="GSM6757150_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385195</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757150_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757150: Stool sRNA-Seq - Patient 28 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870809">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870809</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757150</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757150</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385196" alias="GSM6757151_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385196</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757151_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757151: Stool sRNA-Seq - Patient 28 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870810">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870810</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757151</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757151</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385197" alias="GSM6757168_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385197</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757168_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757168: Stool sRNA-Seq - Patient 33 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870811">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870811</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757168</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757168</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385198" alias="GSM6757169_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385198</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757169_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757169: Stool sRNA-Seq - Patient 33 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870812">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870812</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757169</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757169</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385199" alias="GSM6757170_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385199</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757170_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757170: Stool sRNA-Seq - Patient 4 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870813">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870813</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757170</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757170</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385200" alias="GSM6757171_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385200</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757171_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757171: Stool sRNA-Seq - Patient 4 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870814">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870814</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757171</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757171</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385201" alias="GSM6757172_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385201</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757172_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757172: Stool sRNA-Seq - Patient 4 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870815">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870815</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757172</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757172</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385202" alias="GSM6757173_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385202</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757173_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757173: Stool sRNA-Seq - Patient 6 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870816">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870816</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757173</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757173</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385203" alias="GSM6757174_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385203</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757174_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757174: Stool sRNA-Seq - Patient 6 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870817">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870817</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757174</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757174</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385204" alias="GSM6757175_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385204</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757175_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757175: Stool sRNA-Seq - Patient 6 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870818">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870818</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757175</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757175</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385205" alias="GSM6757176_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385205</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757176_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757176: Stool sRNA-Seq - Patient 7 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870819">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870819</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757176</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757176</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385206" alias="GSM6757177_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385206</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757177_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757177: Stool sRNA-Seq - Patient 7 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870820">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870820</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757177</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757177</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385207" alias="GSM6757178_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385207</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757178_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757178: Stool sRNA-Seq - Patient 7 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870821">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870821</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757178</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757178</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385208" alias="GSM6757179_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385208</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757179_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757179: Stool sRNA-Seq - Patient 8 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870822">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870822</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757179</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757179</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385209" alias="GSM6757180_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385209</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757180_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757180: Stool sRNA-Seq - Patient 8 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870823">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870823</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757180</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757180</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385210" alias="GSM6757181_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385210</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757181_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757181: Stool sRNA-Seq - Patient 8 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870824">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870824</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757181</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757181</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385211" alias="GSM6757182_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385211</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757182_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757182: Stool sRNA-Seq - Patient 9 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870825">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870825</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757182</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757182</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385212" alias="GSM6757183_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385212</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757183_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757183: Stool sRNA-Seq - Patient 9 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870826">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870826</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757183</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757183</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385213" alias="GSM6757152_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385213</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757152_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757152: Stool sRNA-Seq - Patient 29 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870827">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870827</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757152</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757152</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385214" alias="GSM6757153_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385214</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757153_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757153: Stool sRNA-Seq - Patient 29 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870828">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870828</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757153</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757153</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385215" alias="GSM6757154_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385215</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757154_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757154: Stool sRNA-Seq - Patient 29 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870829">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870829</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757154</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757154</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385216" alias="GSM6757155_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385216</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757155_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757155: Stool sRNA-Seq - Patient 2 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870830">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870830</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757155</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757155</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385217" alias="GSM6757156_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385217</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757156_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757156: Stool sRNA-Seq - Patient 2 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870831">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870831</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757156</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757156</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385218" alias="GSM6757157_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385218</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757157_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757157: Stool sRNA-Seq - Patient 2 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870832">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870832</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757157</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757157</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385219" alias="GSM6757158_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385219</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757158_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757158: Stool sRNA-Seq - Patient 30 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870833">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870833</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757158</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757158</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385220" alias="GSM6757159_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385220</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757159_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757159: Stool sRNA-Seq - Patient 30 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870834">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870834</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757159</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757159</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385221" alias="GSM6757160_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385221</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757160_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757160: Stool sRNA-Seq - Patient 30 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870835">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870835</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757160</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757160</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385222" alias="GSM6757161_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385222</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757161_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757161: Stool sRNA-Seq - Patient 31 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870836">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870836</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757161</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757161</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385223" alias="GSM6757162_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385223</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757162_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757162: Stool sRNA-Seq - Patient 31 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870837">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870837</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757162</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757162</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385224" alias="GSM6757163_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385224</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757163_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757163: Stool sRNA-Seq - Patient 31 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870838">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870838</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757163</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757163</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385225" alias="GSM6757164_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385225</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757164_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757164: Stool sRNA-Seq - Patient 32 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870839">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870839</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757164</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757164</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385226" alias="GSM6757165_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385226</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757165_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757165: Stool sRNA-Seq - Patient 32 T1; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870840">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870840</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757165</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757165</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385227" alias="GSM6757166_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385227</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757166_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757166: Stool sRNA-Seq - Patient 32 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870841">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870841</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757166</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757166</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385228" alias="GSM6757167_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385228</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757167_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757167: Stool sRNA-Seq - Patient 33 T0; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870842">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870842</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757167</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757167</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18385229" alias="GSM6757184_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18385229</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6757184_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6757184: Stool sRNA-Seq - Patient 9 T2; Homo sapiens; miRNA-Seq</TITLE>
    <STUDY_REF accession="SRP409976">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP409976</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA905693</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15870843">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15870843</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6757184</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6757184</LIBRARY_NAME>
        <LIBRARY_STRATEGY>miRNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>size fractionation</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Stool RNA was extracted from 200µl aliquots using stool total RNA purification kit (Norgen Biotek Corp.) following manufacturer's protocol. RNA quality and quantity were verified following the MIQE guidelines (http://miqe.gene-quantification.info/). The RNA concentration was quantified with the Qubit microRNA assay kit (Invitrogen). The DNA was extracted with the DNeasy PowerSoil Pro Kit (Qiagen) following manufacturer's instructions with a higher final elution buffer volume (50µl) to increase DNA concentration which was quantified with Qubit DNA high sensitivity assay kit (Invitrogen). Small RNA (sRNA) transcripts were converted into barcoded cDNA libraries. Library preparation was performed with the NEBNext Multiplex Small RNA Library Prep Set for Illumina (Protocol E7330, New England BioLabs Inc., USA).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
