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<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15045318" alias="GSM6076888_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045318</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076888_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076888: Xenopus laevis Embryos, Animal Pole (AP), 5 hpf, Rep 1 [AP_5hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076888</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076888</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045319" alias="GSM6076889_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045319</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076889_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076889: Xenopus laevis Embryos, Animal Pole (AP), 5 hpf, Rep 2 [AP_5hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791473</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076889</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076889</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045320" alias="GSM6076890_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045320</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076890_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076890: Xenopus laevis Embryos, Animal Pole (AP), 5 hpf, Rep 3 [AP_5hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076890</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076890</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045321" alias="GSM6076891_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045321</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076891_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076891: Xenopus laevis Embryos, Animal Pole (AP), 6 hpf, Rep 1 [AP_6hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076891</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076891</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045322" alias="GSM6076892_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045322</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076892_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076892: Xenopus laevis Embryos, Animal Pole (AP), 6 hpf, Rep 2 [AP_6hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076892</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076892</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045323" alias="GSM6076893_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045323</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076893_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076893: Xenopus laevis Embryos, Animal Pole (AP), 6 hpf, Rep 3 [AP_6hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076893</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076893</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045324" alias="GSM6076894_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045324</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076894_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076894: Xenopus laevis Embryos, Animal Pole (AP), 7 hpf, Rep 1 [AP_7hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076894</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076894</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045325" alias="GSM6076895_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045325</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076895_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076895: Xenopus laevis Embryos, Animal Pole (AP), 7 hpf, Rep 2 [AP_7hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076895</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076895</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045326" alias="GSM6076896_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045326</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076896_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076896: Xenopus laevis Embryos, Animal Pole (AP), 7 hpf, Rep 3 [AP_7hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076896</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076896</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045327" alias="GSM6076897_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045327</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076897_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076897: Xenopus laevis Embryos, Animal Pole (AP), 8 hpf, Rep 1 [AP_8hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076897</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076897</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045328" alias="GSM6076898_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045328</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076898_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076898: Xenopus laevis Embryos, Animal Pole (AP), 8 hpf, Rep 2 [AP_8hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791483</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076898</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076898</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045329" alias="GSM6076899_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045329</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076899_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076899: Xenopus laevis Embryos, Animal Pole (AP), 8 hpf, Rep 3 [AP_8hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791484</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076899</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076899</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045330" alias="GSM6076900_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045330</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076900_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076900: Xenopus laevis Embryos, Animal Pole (AP), 9 hpf, Rep 1 [AP_9hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791485">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791485</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076900</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076900</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045331" alias="GSM6076901_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045331</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076901_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076901: Xenopus laevis Embryos, Animal Pole (AP), 9 hpf, Rep 2 [AP_9hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791486">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791486</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076901</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076901</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045332" alias="GSM6076902_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045332</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076902_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076902: Xenopus laevis Embryos, Animal Pole (AP), 9 hpf, Rep 3 [AP_9hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791487">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791487</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076902</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076902</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045333" alias="GSM6076903_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045333</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076903_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076903: Xenopus laevis Embryos, Vegetal Pole (VP), 5 hpf, Rep 1 [VP_5hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791488">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791488</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076903</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076903</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045334" alias="GSM6076920_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045334</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076920_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076920: Xenopus laevis Embryos, Animal Pole (AP), 7 hpf, Rep 4 [AP_7hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791489">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791489</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076920</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045335" alias="GSM6076921_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045335</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076921_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076921: Xenopus laevis Embryos, Animal Pole (AP), 7 hpf, Rep 5 [AP_7hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791490">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791490</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076921</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076921</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045336" alias="GSM6076922_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045336</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076922_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076922: Xenopus laevis Embryos, Animal Pole (AP), 8 hpf, Rep 4 [AP_8hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791491">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791491</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076922</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045337" alias="GSM6076923_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045337</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076923_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076923: Xenopus laevis Embryos, Animal Pole (AP), 8 hpf, Rep 5 [AP_8hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791492">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791492</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076923</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045338" alias="GSM6076924_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045338</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076924_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076924: Xenopus laevis Embryos, Animal Pole (AP), 9 hpf, Rep 4 [AP_9hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791493">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791493</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076924</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076924</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045339" alias="GSM6076925_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045339</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076925_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076925: Xenopus laevis Embryos, Animal Pole (AP), 9 hpf, Rep 5 [AP_9hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791494">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791494</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076925</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076925</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045340" alias="GSM6076926_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045340</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076926_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076926: Xenopus laevis Embryos, Vegetal Pole (VP), 6 hpf, Rep 4 [VP_6hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791495">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791495</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076926</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045341" alias="GSM6076927_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045341</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076927_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076927: Xenopus laevis Embryos, Vegetal Pole (VP), 6 hpf, Rep 5 [VP_6hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791496">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791496</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076927</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045342" alias="GSM6076928_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045342</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076928_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076928: Xenopus laevis Embryos, Vegetal Pole (VP), 7 hpf, Rep 4 [VP_7hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791497">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791497</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076928</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045343" alias="GSM6076929_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045343</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076929_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076929: Xenopus laevis Embryos, Vegetal Pole (VP), 7 hpf, Rep 5 [VP_7hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791499">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791499</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076929</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045344" alias="GSM6076930_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045344</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076930_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076930: Xenopus laevis Embryos, Vegetal Pole (VP), 8 hpf, Rep 4 [VP_8hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791498">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791498</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076930</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045345" alias="GSM6076931_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045345</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076931_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076931: Xenopus laevis Embryos, Vegetal Pole (VP), 8 hpf, Rep 5 [VP_8hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791500">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791500</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076931</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076931</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045346" alias="GSM6076932_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045346</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076932_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076932: Xenopus laevis Embryos, Vegetal Pole (VP), 9 hpf, Rep 4 [VP_9hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791501">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791501</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076932</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045347" alias="GSM6076933_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045347</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076933_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076933: Xenopus laevis Embryos, Vegetal Pole (VP), 9 hpf, Rep 5 [VP_9hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791503">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791503</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076933</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045348" alias="GSM6076904_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045348</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076904_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076904: Xenopus laevis Embryos, Vegetal Pole (VP), 5 hpf, Rep 2 [VP_5hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791502">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791502</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076904</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076904</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045349" alias="GSM6076905_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045349</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076905_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076905: Xenopus laevis Embryos, Vegetal Pole (VP), 5 hpf, Rep 3 [VP_5hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791504">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791504</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076905</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076905</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045350" alias="GSM6076906_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045350</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076906_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076906: Xenopus laevis Embryos, Vegetal Pole (VP), 6 hpf, Rep 1 [VP_6hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791505">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791505</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076906</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076906</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045351" alias="GSM6076907_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045351</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076907_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076907: Xenopus laevis Embryos, Vegetal Pole (VP), 6 hpf, Rep 2 [VP_6hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791506">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791506</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076907</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045352" alias="GSM6076908_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045352</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076908_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076908: Xenopus laevis Embryos, Vegetal Pole (VP), 6 hpf, Rep 3 [VP_6hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791507">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791507</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076908</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045353" alias="GSM6076909_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045353</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076909_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076909: Xenopus laevis Embryos, Vegetal Pole (VP), 7 hpf, Rep 1 [VP_7hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791508">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791508</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076909</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045354" alias="GSM6076910_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045354</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076910_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076910: Xenopus laevis Embryos, Vegetal Pole (VP), 7 hpf, Rep 2 [VP_7hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791509">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791509</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076910</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045355" alias="GSM6076911_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045355</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076911_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076911: Xenopus laevis Embryos, Vegetal Pole (VP), 7 hpf, Rep 3 [VP_7hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791510">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791510</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076911</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076911</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045356" alias="GSM6076912_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045356</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076912_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076912: Xenopus laevis Embryos, Vegetal Pole (VP), 8 hpf, Rep 1 [VP_8hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791512">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791512</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076912</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045357" alias="GSM6076913_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045357</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076913_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076913: Xenopus laevis Embryos, Vegetal Pole (VP), 8 hpf, Rep 2 [VP_8hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791511">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791511</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076913</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045358" alias="GSM6076914_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045358</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076914_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076914: Xenopus laevis Embryos, Vegetal Pole (VP), 8 hpf, Rep 3 [VP_8hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791513">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791513</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076914</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076914</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045359" alias="GSM6076915_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045359</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076915_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076915: Xenopus laevis Embryos, Vegetal Pole (VP), 9 hpf, Rep 1 [VP_9hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791514">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791514</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076915</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076915</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045360" alias="GSM6076916_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045360</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076916_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076916: Xenopus laevis Embryos, Vegetal Pole (VP), 9 hpf, Rep 2 [VP_9hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791515">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791515</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076916</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045361" alias="GSM6076917_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045361</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076917_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076917: Xenopus laevis Embryos, Vegetal Pole (VP), 9 hpf, Rep 3 [VP_9hpf_rep3]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791516">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791516</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076917</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045362" alias="GSM6076918_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045362</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076918_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076918: Xenopus laevis Embryos, Animal Pole (AP), 6 hpf, Rep 4 [AP_6hpf_rep4]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791517">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791517</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076918</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX15045363" alias="GSM6076919_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045363</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076919_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076919: Xenopus laevis Embryos, Animal Pole (AP), 6 hpf, Rep 5 [AP_6hpf_rep5]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372766">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372766</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833149</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791518">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791518</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076919</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were isolated using the RNeasy Mini Kit (Qiagen), following the instructions provided by the manufacturer. Nascent EU-RNAs were biotinylated using bisulfide biotin azide via click reaction and purified using streptavidin beads following the instructions provided by the Click-iTTM Nascent RNA Capture Kit (Thermo Fisher Scientific, Cat# C10365). The cDNA libraries for purified ascent transcripts were prepared using the Universal RNA-seq with NuQuant® kit (NuGEN, Cat# 0364), following the manual provided by the manufacturer. Ribosomal RNAs were depleted using the custom designed AnyDeplete Probe Mix for Xenopus laevis provided by the kit.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
