<?xml version="1.0" encoding="UTF-8"?>
<STUDY_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <STUDY center_name="GEO" alias="GSE180253" accession="SRP328696">
    <IDENTIFIERS>
      <PRIMARY_ID>SRP328696</PRIMARY_ID>
      <EXTERNAL_ID namespace="BioProject" label="primary">PRJNA747271</EXTERNAL_ID>
      <EXTERNAL_ID namespace="GEO">GSE180253</EXTERNAL_ID>
    </IDENTIFIERS>
    <DESCRIPTOR>
      <STUDY_TITLE>m6Am-seq reveals the dynamic m6Am methylation in the human transcriptome</STUDY_TITLE>
      <STUDY_TYPE existing_study_type="Other"/>
      <STUDY_ABSTRACT>We report m6Am-seq, based on selective in vitro demethylation and RNA immunoprecipitation. m6Am-seq directly distinguishes m6Am and 5'-UTR N6-methyladenosine (m6A). Overall design: The mAm-seq is divided into a total of three steps: 1) cap-m7G RNA immunoprecipitation; 2) In vitro demethylation treatment; 3) m6A RNA immunoprecipitation. An m6Am peak could be identified by identifying the demethylase sensitivity peak between the FTO(+) and FTO(-) samples.</STUDY_ABSTRACT>
      <CENTER_PROJECT_NAME>GSE180253</CENTER_PROJECT_NAME>
    </DESCRIPTOR>
    <STUDY_LINKS>
      <STUDY_LINK>
        <XREF_LINK>
          <DB>pubmed</DB>
          <ID>34362929</ID>
        </XREF_LINK>
      </STUDY_LINK>
    </STUDY_LINKS>
  </STUDY>
</STUDY_SET>
