<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T6" accession="SRS165524">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165524</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203910</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 6 (T6)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a CIMP tumor by satisfying the criteria of having DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring BRAF mutation, and is microsatellite unstable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T5" accession="SRS165523">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165523</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203909</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 5 (T5)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a CIMP tumor by satisfying the criteria of having DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring BRAF mutation, and is microsatellite unstable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T4" accession="SRS165522">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165522</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203908</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 4 (T4)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a CIMP tumor by satisfying the criteria of having DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring BRAF mutation, and is microsatellite unstable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T3" accession="SRS165521">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165521</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203907</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 3 (T3)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a non-CIMP tumor by satisfying the criteria of having no DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring KRAS mutation, and is microsatellite stable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T2" accession="SRS165520">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165520</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203906</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 2 (T2)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a non-CIMP tumor by satisfying the criteria of having no DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring KRAS mutation, and is microsatellite stable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE center_name="Cleveland Clinic Foundation" alias="T1" accession="SRS165519">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS165519</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00203905</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Colon cancer sample 1 (T1)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>This is a colon cancer sample from a male patient.  The cancer was defined as a non-CIMP tumor by satisfying the criteria of having no DNA methylation at CACNA1G, IGF2, NEUROG1, RUNX3, and SOCS1, harboring KRAS mutation, and is microsatellite stable.</DESCRIPTION>
  </SAMPLE>
  <SAMPLE alias="N3" center_name="Cleveland Clinic Foundation" accession="SRS161436">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS161436</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00199822</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Normal colon sample 3 (N3)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
    </SAMPLE_NAME>
    <DESCRIPTION/>
  </SAMPLE>
  <SAMPLE alias="N2" center_name="Cleveland Clinic Foundation" accession="SRS161435">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS161435</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00199821</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Normal colon sample 2 (N2)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
    </SAMPLE_NAME>
    <DESCRIPTION/>
  </SAMPLE>
  <SAMPLE alias="N1" center_name="Cleveland Clinic Foundation" accession="SRS161433">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS161433</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN00199819</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Normal colon sample 1 (N1)</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
    </SAMPLE_NAME>
    <DESCRIPTION/>
  </SAMPLE>
</SAMPLE_SET>
