<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX3938576" alias="aa-control-rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938576</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-control-rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - control condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169945">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169945</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D501-D706  Control  Replicate 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-control-rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938577" alias="aa-40mm-rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938577</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-40mm-rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169928">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169928</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D507-D707  40mM HU  Replicate 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-40mm-rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938578" alias="aa-10mm-rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938578</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-10mm-rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169930">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169930</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D501-D712  10mM HU  Replicate 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-10mm-rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938579" alias="aa-5mm-rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938579</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-5mm-rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169931">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169931</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D501-D709 5mM HU  Replicate 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-5mm-rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938580" alias="aa-5mm-rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938580</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-5mm-rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169932">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169932</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D506-D709  5mM HU  Replicate 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-5mm-rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938581" alias="aa-control-rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938581</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-control-rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - control condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169933">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169933</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D506-D702  Control  Replicate 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-control-rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938582" alias="aa-20mm-rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938582</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-20mm-rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169934">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169934</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D506-D711  20mM HU  Replicate 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-20mm-rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938583" alias="aa-10mm-rep1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938583</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-10mm-rep1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169935">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169935</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D506-D710  10mM HU  Replicate 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-10mm-rep1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938584" alias="aa-40mm-rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938584</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-40mm-rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169936">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169936</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D502-D702   40mM HU  Replicate 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-40mm-rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX3938585" alias="aa-20mm-rep2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3938585</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB3906770">aa-20mm-rep2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>PCR amplification of g+d in yeast</TITLE>
    <STUDY_REF accession="SRP140260">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP140260</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB3906770">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>PCR amplification of guide+donor members programmed to create Sgs1 amino acid subsitutions - HU test condition</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3169937">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3169937</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|xiaoge_guo">D501-D711  20mM HU  Replicate 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>aa-20mm-rep2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>AMPLICON</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>OTHER</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>PCR</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
