<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX15045209" alias="GSM6076934_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045209</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076934_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076934: Xenopus laevis Embryos, Control, 5 hpf, Rep 1 [Control_5hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791336">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791336</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076934</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076934</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="SRX15045210" alias="GSM6076935_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045210</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076935_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076935: Xenopus laevis Embryos, Control, 5 hpf, Rep 2 [Control_5hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791531">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791531</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076935</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076935</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="SRX15045211" alias="GSM6076936_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045211</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076936_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076936: Xenopus laevis Embryos, Control, 7.5 hpf, Rep 1 [Control_7.5hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791337">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791337</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076936</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076936</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="SRX15045212" alias="GSM6076937_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045212</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076937_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076937: Xenopus laevis Embryos, Control, 7.5 hpf, Rep 2 [Control_7.5hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791532">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791532</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076937</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076937</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="SRX15045213" alias="GSM6076938_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045213</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076938_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076938: Xenopus laevis Embryos, CHX, 7.5 hpf, Rep 1 [CHX_7.5hpf_rep1]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791338">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791338</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076938</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076938</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="SRX15045214" alias="GSM6076939_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX15045214</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6076939_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6076939: Xenopus laevis Embryos, CHX, 7.5 hpf, Rep 2 [CHX_7.5hpf_rep2]; Xenopus laevis; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP372759">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP372759</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA833148</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS12791339">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS12791339</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6076939</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6076939</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>
