<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15242338" alias="GSM6134097_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242338</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134097_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134097: E14-WT, FBS, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975269">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975269</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134097</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134097</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242339" alias="GSM6134098_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242339</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134098_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134098: E14-Mettl3-KO, FBS, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975270">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975270</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134098</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134098</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242340" alias="GSM6134099_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242340</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134099_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134099: E14-WT, paused, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975271">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975271</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134099</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134099</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242341" alias="GSM6134100_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242341</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134100_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134100: E14-Mettl3-KO, paused, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975272">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975272</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134100</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134100</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242342" alias="GSM6134101_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242342</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134101_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134101: E14-WT, FBS, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975273">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975273</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134101</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134101</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242343" alias="GSM6134102_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242343</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134102_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134102: E14-Mettl3-KO, FBS, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975274">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975274</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134102</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134102</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242344" alias="GSM6134103_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242344</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134103_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134103: E14-WT, paused, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975275">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975275</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134103</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134103</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242345" alias="GSM6134104_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242345</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134104_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134104: E14-Mettl3-KO, paused, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975276">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975276</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134104</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134104</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242346" alias="GSM6134105_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242346</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134105_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134105: E14-WT, FBS, rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975277">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975277</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134105</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134105</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242347" alias="GSM6134106_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242347</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134106_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134106: E14-Mettl3-KO, FBS, rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975278">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975278</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134106</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134106</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242348" alias="GSM6134107_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242348</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134107_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134107: E14-WT, paused, rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975279">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975279</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134107</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134107</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15242349" alias="GSM6134108_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15242349</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6134108_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6134108: E14-Mettl3-KO, paused, rep3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP374922">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP374922</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA837543</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12975280">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12975280</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6134108</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6134108</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>RNA was extracted from equal number of ESCs (2x10^5 cells), with RNeasy Micro Kit with on-column DNase I digestion (QIAGEN). RNA was spiked with synthetic RNAs from the External RNAs Control Consortium (ERCC) Spike-in Mix1 (Thermo Fisher), with 2µl of 1:100 ERCC dilution added to 10µl of RNA, equivalent to ~1-2µg RNA. Library preparation was done using the NEBNext Ultra II Directional Library Prep Kit for Illumina with the mRNA Magnetic Isolation Module from 1µg RNA, per manufacturer's instructions (NEB).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
