<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2860293" accession="SRX3403567">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3403567</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2860293</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2860293: m6A-irCLIP rep1; Mus musculus; OTHER</TITLE>
    <STUDY_REF accession="SRP125187" refname="GSE107055">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125187</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2706144">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2706144</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2860293</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and total RNA collected, RNA was polyA selected, and fragmented to ~30-60 nts, m6A residues were isolated by crosslinking anti-m6A antibody to fragmented RNA RNA ligation for library construction was perfromed on affinity beads and RNA was subsequenctly transformed into dsRNA libraries using RT, cDNA circularization, and PCR amplification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302860293</ID>
          <LABEL>GSM2860293</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2860293</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2860294" accession="SRX3403568">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3403568</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2860294</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2860294: m6A-irCLIP rep2; Mus musculus; OTHER</TITLE>
    <STUDY_REF accession="SRP125187" refname="GSE107055">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125187</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2706146">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2706146</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2860294</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_STRATEGY>OTHER</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>other</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Cells were lysed and total RNA collected, RNA was polyA selected, and fragmented to ~30-60 nts, m6A residues were isolated by crosslinking anti-m6A antibody to fragmented RNA RNA ligation for library construction was perfromed on affinity beads and RNA was subsequenctly transformed into dsRNA libraries using RT, cDNA circularization, and PCR amplification</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302860294</ID>
          <LABEL>GSM2860294</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2860294</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
