<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2865566" accession="SRX3424135">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424135</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865566</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865566: ZF4-28 rep1; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715769">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715769</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865566</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865566</ID>
          <LABEL>GSM2865566</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865566</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865567" accession="SRX3424136">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424136</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865567</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865567: ZF4-28 rep2; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715767">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715767</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865567</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865567</ID>
          <LABEL>GSM2865567</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865567</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865568" accession="SRX3424137">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424137</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865568</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865568: ZF4-28 rep3; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715768">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715768</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865568</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865568</ID>
          <LABEL>GSM2865568</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865568</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865569" accession="SRX3424138">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424138</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865569</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865569: ZF4-18-30d rep1; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715770">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715770</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865569</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865569</ID>
          <LABEL>GSM2865569</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865569</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865570" accession="SRX3424139">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424139</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865570</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865570: ZF4-18-30d rep2; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715771">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715771</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865570</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865570</ID>
          <LABEL>GSM2865570</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865570</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2865571" accession="SRX3424140">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3424140</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2865571</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2865571: ZF4-18-30d rep3; Danio rerio; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125677" refname="GSE107369">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125677</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2715772">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2715772</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2865571</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <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 RNA was extracted using miRNeasy Mini Kit (217004, Qiagen) and purified by RNAClean XP Kit (A63987, Beckman Coulter) and RNase-Free DNase Set (79254, Qiagen). Libraries were constructed using the TruSeq Stranded Total RNA LT Sample Prep Kit with Ribo-Zero (RS-122-2301/ RS-122-2302, Illumina). Libraries were pooled and sequenced using the Illumina HiSeq machine as 150-bp paired-end sequencing reads.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>HiSeq X Ten</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302865571</ID>
          <LABEL>GSM2865571</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2865571</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
