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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15948603" alias="nnn15_noa1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948603</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_noa1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, untreated, replicate 1</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635426">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635426</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_noa1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_noa1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15948604" alias="nnn15_noa2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948604</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_noa2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, untreated, replicate 2</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635428">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635428</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_noa2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_noa2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15948605" alias="nnn15_noa3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948605</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_noa3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, untreated, replicate 3</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635427">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635427</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_noa3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_noa3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15948606" alias="nnn15_tcx1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948606</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_tcx1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, treated with 100 M tretacenomycin X, replicate 1</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635429">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635429</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_tcx1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_tcx1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15948607" alias="nnn15_tcx2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948607</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_tcx2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, treated with 100 M tretacenomycin X, replicate 2</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635430">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635430</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_tcx2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_tcx2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15948608" alias="nnn15_tcx3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15948608</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB11420518">nnn15_tcx3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>NNN15 library, treated with 100 M tretacenomycin X, replicate 3</TITLE>
    <STUDY_REF accession="SRP384293">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP384293</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB11420518">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing adapter were added to the ds cDNA obtained after iTP-Seq (inverse toeprinting) by PCR. PCR products were then purified using a PCR purification kit, checked for quality and quantity with BioAnalyzer 2100 using the DNA1000 kit.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS13635431">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS13635431</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|ttr@orcid">nnn15_tcx3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>nnn15_tcx3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>SYNTHETIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
