<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE32307" accession="SRP008331">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP008331</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA147303</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE32307</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>Transposon-based construction of strand-specific RNA-seq libraries</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Transcriptome Analysis"/>
      <STUDY_ABSTRACT>We have developed two methods for efficiently consructing RNA-seq libraries using transposition.  Each method constructs high quality RNA-seq libraries when compared to standard approaches. One of the methods (Directional Tn-RNA-seq) maintains strand-of-origin information and exhibits strand specificity comparable to current approaches. Overall design: RNA-seq libraries were constructed from ECC-1, a human cell line, and Universal Human Reference RNA using transposon-based and standard RNA-seq library construciton methods.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE32307</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>22128135</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
