<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE202353" accession="SRP373924">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP373924</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA835699</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE202353</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>NOMe-Seq analysis of IMR-90 cell line II</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Whole Genome Sequencing"/>
      <STUDY_ABSTRACT>NOMe-Seq analysis was performed with GC-recognizing cytosine DNA methyltransferase Overall design: The IMR-90 nuclei were prepared with a solution containing 0.1% NP-40. Then, the nuclei were suspended in methylation buffer, and cytosine C-5 DNA methyltransferase recognizing GC dinucleotide was added. The solution was incubated at 37°C for 1 hr and collected nuclei. Then genomic DNA was extracted, and library preparation was performed with tPBAT protocol (Miura F et al., NAR, 2019)</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE202353</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>36333700</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
