<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_4791_5" center_name="SC" accession="ERX010186">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX010186</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4791_5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE/>
    <STUDY_REF accession="ERP000500" refname="Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000500</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of barcoded sample library "F12_Mock_R2" for the "Rapid high-resolution QTL mapping in yeast" study. Only first read of the read pair produced good quality data, the second read should be discarded.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS018249" refname="Yeast-sc-2011-01-25-35139" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS018249</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Yeast-sc-2011-01-25-35139</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F12_Mock_R2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="275"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>No PCR</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>160</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>barcode_tag</READ_LABEL>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>BarCode</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>85</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <PROCESSING/>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_4791_3" center_name="SC" accession="ERX010187">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX010187</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4791_3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE/>
    <STUDY_REF accession="ERP000500" refname="Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000500</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of barcoded sample library "F12_Mock_R1" for the "Rapid high-resolution QTL mapping in yeast" study. Only first read of the read pair produced good quality data, the second read should be discarded.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS018247" refname="Yeast-sc-2011-01-25-35137" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS018247</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Yeast-sc-2011-01-25-35137</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F12_Mock_R1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="275"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>No PCR</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>160</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>barcode_tag</READ_LABEL>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>BarCode</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>85</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <PROCESSING/>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_4791_6" center_name="SC" accession="ERX010188">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX010188</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_4791_6</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE/>
    <STUDY_REF accession="ERP000500" refname="Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP000500</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Rapid_high_resolution_QTL_mapping_in_yeast-sc-2011-01-25</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of barcoded sample library "F12_Heat_R1_T4" for the "Rapid high-resolution QTL mapping in yeast" study. Only first read of the read pair produced good quality data, the second read should be discarded.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS018252" refname="Yeast-sc-2011-01-25-35142" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS018252</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">Yeast-sc-2011-01-25-35142</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>F12_Heat_R1_T4</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WGS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="275"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>No PCR</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>160</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>1</READ_INDEX>
            <READ_LABEL>barcode_tag</READ_LABEL>
            <READ_CLASS>Technical Read</READ_CLASS>
            <READ_TYPE>BarCode</READ_TYPE>
            <BASE_COORD>77</BASE_COORD>
          </READ_SPEC>
          <READ_SPEC>
            <READ_INDEX>2</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Reverse</READ_TYPE>
            <BASE_COORD>85</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina Genome Analyzer II</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <PROCESSING/>
  </EXPERIMENT>
</EXPERIMENT_SET>
