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      <PRIMARY_ID>SRX5294524</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5067990">GCMSC</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ERCC6 GC MSC</TITLE>
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        <PRIMARY_ID>SRP174074</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>DNA was randomly fragmented using a Covaris ultrasonic processor. Fragmented DNA was ligated with DNA adaptors (Illumina) and amplified using Illumina paired-end PCR primers. DNA libraries were quantified using a Qubit 2.0 Fluorometer (Life Technologies) and analysed using an Agilent Bioanalyzer 2100 to determine the insert sizes of the fragments in the libraries. The library of fragments was sequenced on an Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
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      <PRIMARY_ID>SRX5294525</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5067990">4iPSC</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ERCC6 mut iPSC</TITLE>
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        <PRIMARY_ID>SRP174074</PRIMARY_ID>
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      <DESIGN_DESCRIPTION>DNA was randomly fragmented using a Covaris ultrasonic processor. Fragmented DNA was ligated with DNA adaptors (Illumina) and amplified using Illumina paired-end PCR primers. DNA libraries were quantified using a Qubit 2.0 Fluorometer (Life Technologies) and analysed using an Agilent Bioanalyzer 2100 to determine the insert sizes of the fragments in the libraries. The library of fragments was sequenced on an Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4293783</PRIMARY_ID>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5294526</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5067990">CS-fib</SUBMITTER_ID>
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    <TITLE>ERCC6 mut fibroblast</TITLE>
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      <DESIGN_DESCRIPTION>DNA was randomly fragmented using a Covaris ultrasonic processor. Fragmented DNA was ligated with DNA adaptors (Illumina) and amplified using Illumina paired-end PCR primers. DNA libraries were quantified using a Qubit 2.0 Fluorometer (Life Technologies) and analysed using an Agilent Bioanalyzer 2100 to determine the insert sizes of the fragments in the libraries. The library of fragments was sequenced on an Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4293784</PRIMARY_ID>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5294527</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5067990">4MSC</SUBMITTER_ID>
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    <TITLE>ERCC6 mut MSC</TITLE>
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        <PRIMARY_ID>SRP174074</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA510990</EXTERNAL_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was randomly fragmented using a Covaris ultrasonic processor. Fragmented DNA was ligated with DNA adaptors (Illumina) and amplified using Illumina paired-end PCR primers. DNA libraries were quantified using a Qubit 2.0 Fluorometer (Life Technologies) and analysed using an Agilent Bioanalyzer 2100 to determine the insert sizes of the fragments in the libraries. The library of fragments was sequenced on an Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
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          <PRIMARY_ID>SRS4293785</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|pekingysu">4MSC</SUBMITTER_ID>
        </IDENTIFIERS>
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        <LIBRARY_NAME>4MSC</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
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          <PAIRED/>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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      <PRIMARY_ID>SRX5294528</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB5067990">GCiPSC</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>ERCC6 GC iPSC</TITLE>
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        <PRIMARY_ID>SRP174074</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA510990</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>DNA was randomly fragmented using a Covaris ultrasonic processor. Fragmented DNA was ligated with DNA adaptors (Illumina) and amplified using Illumina paired-end PCR primers. DNA libraries were quantified using a Qubit 2.0 Fluorometer (Life Technologies) and analysed using an Agilent Bioanalyzer 2100 to determine the insert sizes of the fragments in the libraries. The library of fragments was sequenced on an Illumina HiSeq X Ten platform.</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS4293786</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|pekingysu">GCiPSC</SUBMITTER_ID>
        </IDENTIFIERS>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GCiPSC</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
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        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
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