<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY alias="DRP000374" center_name="OSAKAMED" accession="DRP000374">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB2318</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>A novel transposon-based approach to analyze the 3D structure of the mouse genome in the cell nucleus.</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other" new_study_type="vector insertion site analysis"/>
            <STUDY_ABSTRACT>The 3D organization of the genome has recently been considered to have essential impact on nuclear functions such as gene expression and epigenetic modifications. In this project, we develop a novel application of next-generation sequencing technology to analyze the 3D genome organization in the cell nucleus, in combination with a transposon-based genome engineering approach.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>OSAKAMED</CENTER_PROJECT_NAME>
            <STUDY_DESCRIPTION>Most DNA transposons have a tendency to jump around locally in the genome, referred to as “local hopping” tendency. By using next-generation sequencing technology, we globally identify the transposon insertion sites in a genome-wide manner, and investigate the correlation between the distribution of transposons and the spatial organization of the genome.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
        <STUDY_LINKS>
            <STUDY_LINK>
                <URL_LINK>
                    <LABEL>MEXT Genome Support Project</LABEL>
                    <URL>http://www.genome-sci.jp/</URL>
                </URL_LINK>
            </STUDY_LINK>
        </STUDY_LINKS>
        <STUDY_ATTRIBUTES>
            <STUDY_ATTRIBUTE>
                <TAG>grant</TAG>
                <VALUE>KAKENHI on Innovative Areas - Genome Support Project</VALUE>
            </STUDY_ATTRIBUTE>
        </STUDY_ATTRIBUTES>
    </STUDY>
</STUDY_SET>
