<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM3593755" accession="SRX5346155">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346155</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593755</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593755: TRES_blood_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337886">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337886</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593755</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593755</ID>
          <LABEL>GSM3593755</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593755</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593756" accession="SRX5346156">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346156</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593756</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593756: TRES_ovary_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337887">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337887</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593756</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593756</ID>
          <LABEL>GSM3593756</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593756</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593757" accession="SRX5346157">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346157</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593757</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593757: TRES_brain_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337888">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337888</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593757</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593757</ID>
          <LABEL>GSM3593757</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593757</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593758" accession="SRX5346158">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346158</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593758</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593758: TRES_liver_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337889">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337889</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593758</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593758</ID>
          <LABEL>GSM3593758</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593758</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593759" accession="SRX5346159">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346159</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593759</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593759: TRES_spleen_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337890">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337890</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593759</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593759</ID>
          <LABEL>GSM3593759</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593759</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593760" accession="SRX5346160">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346160</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593760</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593760: TRES_muscle_NextSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337891">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337891</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593760</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593760</ID>
          <LABEL>GSM3593760</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593760</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593761" accession="SRX5346161">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346161</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593761</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593761: TRES_blood_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337892">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337892</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593761</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593761</ID>
          <LABEL>GSM3593761</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593761</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593762" accession="SRX5346162">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346162</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593762</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593762: TRES_ovary_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337893">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337893</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593762</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593762</ID>
          <LABEL>GSM3593762</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593762</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593763" accession="SRX5346163">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346163</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593763</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593763: TRES_brain_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337894">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337894</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593763</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593763</ID>
          <LABEL>GSM3593763</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593763</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593764" accession="SRX5346164">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346164</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593764</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593764: TRES_liver_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337895">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337895</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593764</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593764</ID>
          <LABEL>GSM3593764</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593764</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593765" accession="SRX5346165">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346165</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593765</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593765: TRES_spleen_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337896">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337896</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593765</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593765</ID>
          <LABEL>GSM3593765</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593765</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM3593766" accession="SRX5346166">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX5346166</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM3593766</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM3593766: TRES_muscle_MiSeq; Tachycineta bicolor; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP184473" refname="GSE126210">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP184473</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS4337897">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS4337897</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM3593766</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>Tissues were removed, flash frozen on dry ice, and total RNA was extracted using Trizol reagent. TruSeq Stranded mRNA LT Sample Prep Kit (Illumina) was used for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols; however, when preparing larger fragments, the fragmentation step was reduced from 8min to 10s at 94oC.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina MiSeq</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>303593766</ID>
          <LABEL>GSM3593766</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM3593766</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
