<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY alias="DRP007621" center_name="HIROSHIMA" accession="DRP007621">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB10583</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>Chromatin immunoprecipitation of HB1119 cells.</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>Chromatin immunoprecipitation of HB1119 cells was performed using fractionation-assisted native chromatin immunoprecipitation method. Specific antibodies for HBO1, PHF16, MEAF6, ING4, RNAP2 Ser5-P and RNAP2 non-P were used for IP. The ChIPed DNAs were analyzed by deep sequencing along with the input sample.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>Chromatin immunoprecipitation of HB1119 cells.</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB10583</ID>
                        <LABEL>PRJDB10583</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>Chromatin immunoprecipitation of HB1119 cells was performed using fractionation-assisted native chromatin immunoprecipitation method. Specific antibodies for HBO1, PHF16, MEAF6, ING4, RNAP2 Ser5-P and RNAP2 non-P were used for IP. The ChIPed DNAs were analyzed by deep sequencing along with the input sample.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
