<?xml version="1.0" encoding="UTF-8"?>
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  <SAMPLE alias="SAMEA8521030" accession="ERS6205820">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS6205820</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521030</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>ETT1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
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        <VALUE>2021-04-14</VALUE>
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        <VALUE>2021-04-06</VALUE>
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        <TAG>External Id</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
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        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
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        <VALUE>2021-04-14T00:24:52Z</VALUE>
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        <VALUE>2021-04-06T13:32:25Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-10321:ETT1</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
        <VALUE>47</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <SAMPLE_ATTRIBUTE>
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  <SAMPLE alias="SAMEA8521031" accession="ERS6205821">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS6205821</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521031</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>ETT2</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
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        <TAG>External Id</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
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        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
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        <VALUE>2021-04-14T00:24:52Z</VALUE>
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        <TAG>INSDC status</TAG>
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        <VALUE>E-MTAB-10321:ETT2</VALUE>
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        <TAG>age</TAG>
        <VALUE>51</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
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        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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        <TAG>sex</TAG>
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      <PRIMARY_ID>ERS6205822</PRIMARY_ID>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
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        <VALUE>2021-04-14</VALUE>
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        <TAG>ENA last update</TAG>
        <VALUE>2021-04-06</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA8521032</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
        <VALUE>Mayo Clinic</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2021-04-14T00:24:52Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2021-04-06T13:32:26Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-10321:ETT3</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
        <VALUE>46</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>disease</TAG>
        <VALUE>epithelioid trophoblastic tumor</VALUE>
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        <TAG>sex</TAG>
        <VALUE>female</VALUE>
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  <SAMPLE alias="SAMEA8521033" accession="ERS6205823">
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      <PRIMARY_ID>ERS6205823</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521033</EXTERNAL_ID>
    </IDENTIFIERS>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
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        <TAG>ENA last update</TAG>
        <VALUE>2021-04-06</VALUE>
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        <TAG>External Id</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
        <VALUE>Mayo Clinic</VALUE>
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        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2021-04-14T00:24:52Z</VALUE>
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        <TAG>INSDC last update</TAG>
        <VALUE>2021-04-06T13:32:26Z</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-10321:PSN1</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
        <VALUE>36</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>disease</TAG>
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        <TAG>individual</TAG>
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        <TAG>sample name</TAG>
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        <TAG>sex</TAG>
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  <SAMPLE alias="SAMEA8521034" accession="ERS6205824">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS6205824</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521034</EXTERNAL_ID>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
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        <TAG>External Id</TAG>
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        <TAG>INSDC center alias</TAG>
        <VALUE>Mayo Clinic</VALUE>
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        <VALUE>Mayo Clinic</VALUE>
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        <VALUE>2021-04-14T00:24:52Z</VALUE>
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        <TAG>INSDC status</TAG>
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      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
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        <VALUE>26</VALUE>
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        <TAG>broker name</TAG>
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        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <PRIMARY_ID>ERS6205825</PRIMARY_ID>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
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    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
        <VALUE>Mayo Clinic</VALUE>
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        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2021-04-14T00:24:52Z</VALUE>
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        <TAG>INSDC last update</TAG>
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        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
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        <TAG>age</TAG>
        <VALUE>34</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
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        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <SAMPLE_ATTRIBUTE>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERS6205827</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521037</EXTERNAL_ID>
    </IDENTIFIERS>
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      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
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        <TAG>INSDC last update</TAG>
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        <VALUE>public</VALUE>
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        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-10321:PSTT2</VALUE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>human</VALUE>
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      <SAMPLE_ATTRIBUTE>
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      <SAMPLE_ATTRIBUTE>
        <TAG>individual</TAG>
        <VALUE>PSTT2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>organism part</TAG>
        <VALUE>uterus</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-10321:PSTT2</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
  <SAMPLE alias="SAMEA8521036" accession="ERS6205826">
    <IDENTIFIERS>
      <PRIMARY_ID>ERS6205826</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioSample">SAMEA8521036</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>PSTT1</TITLE>
    <SAMPLE_NAME>
      <TAXON_ID>9606</TAXON_ID>
      <SCIENTIFIC_NAME>Homo sapiens</SCIENTIFIC_NAME>
    </SAMPLE_NAME>
    <DESCRIPTION>Protocols: Sections of formalin-fixed paraffin-embedded (FFPE) tissue were freshly cut for nucleic acid extraction. RNA was extracted from FFPE tissue sections using the AllPrep DNA/RNA FFPE Kit (Qiagen, Netherlands) according to the manufacturer's protocol. RNA was eluted in 20-30 µl RNase-free water. DNA and RNA concentrations were quantified using Qubit fluorometry (Invitrogen, Carlsbad, CA). Sequencing libraries were prepared according to manufacturer's instructions for either the TruSeq RNA Sample Prep Kit v2 or the TruSeq RNA Access Library Prep Kit (Illumina, San Diego, CA). Library concentration and size distribution were initially determined using an Agilent Bioanalyzer DNA 1000 chip (Santa Clara, CA), and Qubit fluorometry (Invitrogen, Carlsbad, CA) was performed to confirm concentration.</DESCRIPTION>
    <SAMPLE_ATTRIBUTES>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA first public</TAG>
        <VALUE>2021-04-14</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>ENA last update</TAG>
        <VALUE>2021-04-06</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>External Id</TAG>
        <VALUE>SAMEA8521036</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center alias</TAG>
        <VALUE>Mayo Clinic</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC center name</TAG>
        <VALUE>Mayo Clinic</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC first public</TAG>
        <VALUE>2021-04-14T00:24:52Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC last update</TAG>
        <VALUE>2021-04-06T13:32:26Z</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>INSDC status</TAG>
        <VALUE>public</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>Submitter Id</TAG>
        <VALUE>E-MTAB-10321:PSTT1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>age</TAG>
        <VALUE>41</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>broker name</TAG>
        <VALUE>ArrayExpress</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>common name</TAG>
        <VALUE>human</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>disease</TAG>
        <VALUE>placental site trophoblastic tumor</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>individual</TAG>
        <VALUE>PSTT1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>organism part</TAG>
        <VALUE>uterus</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sample name</TAG>
        <VALUE>E-MTAB-10321:PSTT1</VALUE>
      </SAMPLE_ATTRIBUTE>
      <SAMPLE_ATTRIBUTE>
        <TAG>sex</TAG>
        <VALUE>female</VALUE>
      </SAMPLE_ATTRIBUTE>
    </SAMPLE_ATTRIBUTES>
  </SAMPLE>
</SAMPLE_SET>
