<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE69651" accession="SRP059233">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP059233</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA286101</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE69651</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Genome-wide DNase-seq profiling of Saccharomyces cerevisiae (W303 strain)</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Intact nuclei from an asynchronous population of W303 Saccharomyces cerevisiae in log-phase growth were subjected to a 16-minute DNase I digestion (0.1 U/µL) at 37 °C.  DNA was then recovered, and single-end Illumina sequencing libraries were prepared using the Crawford DNase-seq method (Song and Crawford, 2010). Overall design: Two biological replicates of DNase-seq were sequenced in single-end mode on an Illumina HiSeq 2000.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE69651</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>26772197</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
