<?xml version="1.0" encoding="UTF-8"?>
<SAMPLE_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <SAMPLE alias="NWD348805" accession="SRS1357917">
    <IDENTIFIERS>
      <PRIMARY_ID>SRS1357917</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMN04109193</EXTERNAL_ID>
      <EXTERNAL_ID namespace="dbGaP" label="Sample name">956-NWD348805</EXTERNAL_ID>
      <EXTERNAL_ID namespace="phs000956" label="submitted sample id">NWD348805</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>Non-tumor DNA sample from Blood of a human female participant in the dbGaP study "NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish"</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_accession</TAG>
        <VALUE>phs000956</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitter handle</TAG>
        <VALUE>TOPMed_WGS_Amish</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository</TAG>
        <VALUE>TOPMed_WGS_Amish</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study name</TAG>
        <VALUE>NHLBI TOPMed: Genetics of Cardiometabolic Health in the Amish</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>study design</TAG>
        <VALUE>Family/Twin/Trios</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>biospecimen repository sample id</TAG>
        <VALUE>NWD348805</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted sample id</TAG>
        <VALUE>NWD348805</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>submitted subject id</TAG>
        <VALUE>DBG00667</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_sample_id</TAG>
        <VALUE>1784221</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_subject_id</TAG>
        <VALUE>674062</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>body site</TAG>
        <VALUE>Blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>histological type</TAG>
        <VALUE>Blood</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>analyte type</TAG>
        <VALUE>DNA</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>is tumor</TAG>
        <VALUE>No</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP Genotypes (Array)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>molecular data type</TAG>
        <VALUE>SNP/CNV Genotypes (NGS)</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_code</TAG>
        <VALUE>2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>gap_consent_short_name</TAG>
        <VALUE>HMB-IRB-MDS</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
</SAMPLE_SET>
