<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY alias="ena-STUDY-UCB-09-07-2015-17:58:53:566-495" center_name="UCB" accession="ERP010992">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP010992</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB9845</EXTERNAL_ID>
      <SUBMITTER_ID namespace="UCB">ena-STUDY-UCB-09-07-2015-17:58:53:566-495</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>De novo genome assembly of IFO0880 using Pacbio data</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>Genomic DNA from IFO0880 was prepared by a combination of glass bead lysis, phenol-chloroform extraction, and Qiagen column purification.  A ~20kbp insert library was sequenced using Pacbio technology.  De novo genome assembly of strain IFO0880 (Rhodosporidium toruloides) was performed using the HGAP3 algorithm (part of the Pacbio SMRT Analysis package).</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>Rhodosporidium toruloides IFO0880 Pacbio scaffolds</CENTER_PROJECT_NAME>
      <STUDY_DESCRIPTION>Genomic DNA from IFO0880 was prepared by a combination of glass bead lysis, phenol-chloroform extraction, and Qiagen column purification.  A ~20kbp insert library was sequenced using Pacbio technology.  De novo genome assembly of strain IFO0880 (Rhodosporidium toruloides) was performed using the HGAP3 algorithm (part of the Pacbio SMRT Analysis package).</STUDY_DESCRIPTION>
    </DESCRIPTOR>
  </STUDY>
</STUDY_SET>
