<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY accession="DRP000447" center_name="NIAS" alias="DRP000447">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB2602</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>Transcriptome analysis of Oryza rufipogon W1943 using mRNA-seq</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Transcriptome Sequencing"/>
            <STUDY_ABSTRACT>We analyzed transcriptome in the whole plant body of Oryza rufipogon W1943 using mRNA-seq. Wild rice O. rufipogon W1943 was cultured after protocols from Oryzabase (http://www.shigen.nig.ac.jp/rice/oryzabase/nbrpStrains/nigProtocol.jsp). Seeds of O. rufipogon W1943 were treated at 45 C for 10 days for breaking dormancy. Then the seeds were dehulled and steriled with a fungicidal reagents. Young seedlings were then grown for a week on a moist filter paper in petri dishes in a growth incubator (partial shade). Total plants were flash-frozen in  liquid nitrogen and stored at -80 C until they were used. Total RNAs were prepared from the whole plants with RNeasy Plant Mini Kit (Qiagen, Valencia, CA USA). Total RNAs were then processed with mRNA-seq Kit for producing cDNA libraries for short-read sequencing at Illumina Inc. (Hayward, CA USA)</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>RTR0001</CENTER_PROJECT_NAME>
            <STUDY_DESCRIPTION>none provided</STUDY_DESCRIPTION>
        </DESCRIPTOR>
        <STUDY_LINKS>
            <STUDY_LINK>
                <URL_LINK>
                    <LABEL>Linked publication</LABEL>
                    <URL>http://dx.doi.org/10.1093/molbev/msr315</URL>
                </URL_LINK>
            </STUDY_LINK>
            <STUDY_LINK>
                <XREF_LINK>
                    <DB>pubmed</DB>
                    <ID>22319137</ID>
                </XREF_LINK>
            </STUDY_LINK>
        </STUDY_LINKS>
    </STUDY>
</STUDY_SET>
