<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY accession="DRP002377" center_name="KYUSH-MS" alias="DRP002377">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB2884</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>PBAT-mediated targeted methylome sequencing</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>To enhance the sensitivity of DNA methylome analysis of DNA enriched with hybridization capture technology, a  strategy termed post-bisulfite adaptor tagging (PBAT) was applied. This  enabled targeted methylome analysis from as little as 30 ng of starting DNA extracted from human and mouse.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>PBAT-mediated targeted methylome sequencing</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB2884</ID>
                        <LABEL>PRJDB2884</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>To enhance the sensitivity of DNA methylome analysis of DNA enriched with hybridization capture technology, a  strategy termed post-bisulfite adaptor tagging (PBAT) was applied. This  enabled targeted methylome analysis from as little as 30 ng of starting DNA extracted from human and mouse.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
