<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE125332" accession="SRP180236">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP180236</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA515877</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE125332</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Effects of inhibiting sphingolipid synthesis and TOR signaling on the Candida albicans transcriptome</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>Goal: We employed RNA-seq to detect changes in the transcriptome of the yeast Candida albicans in response to the addition of myriocin, a sphingolipid synthesis inhibitor, or caffeine, a drug that blocks the TOR kinase. The effects of the drugs were studied in wild-type cells and in the rtg3 mutant strain. Overall design: Comparison of the transcriptome of two Candida albicans strains: wild-type and rtg3 deletion mutant. RNA was prepared from each strain grown under three different conditions: no drug added, addition of myriocin or addition of caffeine. Two biological replicates per strain per condition. RNA-seq data generated with Illumina HiSeq2500.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE125332</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
