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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX4930699" alias="Cg_gln3_R1">
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      <PRIMARY_ID>SRX4930699</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_gln3_R1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: gln3 mutant strain</TITLE>
    <STUDY_REF accession="SRP166760">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3975651">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975651</PRIMARY_ID>
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        <LIBRARY_NAME>Cg_gln3_R1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>SRX4930700</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_WT_R3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: WT strain</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4635570">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3975652">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975652</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|luisfernandgar@gmail.com">WT_R3</SUBMITTER_ID>
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        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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  </EXPERIMENT>
  <EXPERIMENT accession="SRX4930701" alias="Cg_WT_R2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4930701</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_WT_R2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: WT strain</TITLE>
    <STUDY_REF accession="SRP166760">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4635570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3975653">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975653</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|luisfernandgar@gmail.com">WT_R2</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cg_WT_R2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
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          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
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  </EXPERIMENT>
  <EXPERIMENT accession="SRX4930702" alias="Cg_WT_R1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4930702</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_WT_R1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: WT strain</TITLE>
    <STUDY_REF accession="SRP166760">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4635570">bp0</SUBMITTER_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975656</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|luisfernandgar@gmail.com">WT_R1</SUBMITTER_ID>
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        <LIBRARY_NAME>Cg_WT_R1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4930703" alias="Cg_gln3_R3">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4930703</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_gln3_R3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: gln3 mutant strain</TITLE>
    <STUDY_REF accession="SRP166760">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4635570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3975654">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975654</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|luisfernandgar@gmail.com">gln3_R3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cg_gln3_R3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX4930704" alias="Cg_gln3_R2">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX4930704</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB4635570">Cg_gln3_R2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>RNA-seq of Candida glagrata: gln3 mutant strain</TITLE>
    <STUDY_REF accession="SRP166760">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP166760</PRIMARY_ID>
        <SUBMITTER_ID namespace="SUB4635570">bp0</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Six independent yeast cultures (3 for WT and 3 for gln3  strains) were grown overnight in YPD media on a roller drum with constant spinning, then cells were washed twice and suspended in 1 ml of sterile milliQ water. Flasks containing 50 ml of MM, were inoculated at OD600 nm 0.1, and incubated at 30 C with constant shaking (220 rpm) until OD600 nm 0.8 to 1.0 was reached. Cells then were pelleted, rapidly transferred to liquid nitrogen, and stored at -80 C. RNA extraction, cDNA library construction and sequencing were performed by the Beijing Genomics Institute (BGI) (Hong Kong, China).</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS3975655">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS3975655</PRIMARY_ID>
          <SUBMITTER_ID namespace="pda|luisfernandgar@gmail.com">gln3_R2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>Cg_gln3_R2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
