<?xml version="1.0" encoding="UTF-8" standalone="yes"?>
<STUDY_SET>
    <STUDY alias="DRP003704" center_name="RIKEN_ACCC" accession="DRP003704">
        <IDENTIFIERS>
            <PRIMARY_ID label="BioProject ID">PRJDB3399</PRIMARY_ID>
        </IDENTIFIERS>
        <DESCRIPTOR>
            <STUDY_TITLE>Validation of single-cell RNA-seq methods</STUDY_TITLE>
            <STUDY_TYPE existing_study_type="Other"/>
            <STUDY_ABSTRACT>Recently, various single-cell RNA-seq methods have been reported. However, almost reported methods cannot detect non-poly-A RNA. In this project, we developed novel single-cell RNA-seq methods, which can detect non-poly-A RNA. To validate quantitative performances of respective methods, we prepared sequence library DNA using purified 10 pg total RNA, respectively. Goal of this project is establishment of quantitative single-cell RNA-seq method, which can detect non-poly-A RNA.</STUDY_ABSTRACT>
            <CENTER_PROJECT_NAME>Validation of single-cell RNA-seq methods</CENTER_PROJECT_NAME>
            <RELATED_STUDIES>
                <RELATED_STUDY>
                    <RELATED_LINK>
                        <DB>bioproject</DB>
                        <ID>PRJDB3399</ID>
                        <LABEL>PRJDB3399</LABEL>
                    </RELATED_LINK>
                    <IS_PRIMARY>true</IS_PRIMARY>
                </RELATED_STUDY>
            </RELATED_STUDIES>
            <STUDY_DESCRIPTION>Recently, various single-cell RNA-seq methods have been reported. However, almost reported methods cannot detect non-poly-A RNA. In this project, we developed novel single-cell RNA-seq methods, which can detect non-poly-A RNA. To validate quantitative performances of respective methods, we prepared sequence library DNA using purified 10 pg total RNA, respectively. Goal of this project is establishment of quantitative single-cell RNA-seq method, which can detect non-poly-A RNA.</STUDY_DESCRIPTION>
        </DESCRIPTOR>
    </STUDY>
</STUDY_SET>
