<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY accession="ERP123797" alias="ena-STUDY-SHANGHAI JIAOTONG UNIVERSITY SCHOOL OF MEDICINE-03-09-2020-04:42:20:549-790" center_name="SHANGHAI JIAOTONG UNIVERSITY SCHOOL OF MEDICINE">
    <IDENTIFIERS>
      <PRIMARY_ID>ERP123797</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject">PRJEB40185</EXTERNAL_ID>
      <SUBMITTER_ID namespace="SHANGHAI JIAOTONG UNIVERSITY SCHOOL OF MEDICINE">ena-STUDY-SHANGHAI JIAOTONG UNIVERSITY SCHOOL OF MEDICINE-03-09-2020-04:42:20:549-790</SUBMITTER_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>ATAC-seq in human CD4+T cells, CD8+T cells, CD19+B cells and CD14+ monocytes</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>To test the chromatin accessibility of different immune cell subsets, we isolated CD4+T cells, CD8+T cells, CD19+B cells and CD14+ monocytes from human PBMCs and performed ATAC assay.</STUDY_ABSTRACT>
      <STUDY_DESCRIPTION>To test the chromatin accessibility of different immune cell subsets, we isolated CD4+T cells, CD8+T cells, CD19+B cells and CD14+ monocytes from human PBMCs and performed ATAC assay.</STUDY_DESCRIPTION>
    </DESCRIPTOR>
    <STUDY_ATTRIBUTES>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-FIRST-PUBLIC</TAG>
        <VALUE>2021-01-05</VALUE>
      </STUDY_ATTRIBUTE>
      <STUDY_ATTRIBUTE>
        <TAG>ENA-LAST-UPDATE</TAG>
        <VALUE>2020-09-03</VALUE>
      </STUDY_ATTRIBUTE>
    </STUDY_ATTRIBUTES>
  </STUDY>
</STUDY_SET>
