<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX17952594" alias="GSM6658034_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17952594</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658034_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658034: hypothalamus, WD, Tas1r3-/-, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA891954</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15469799">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15469799</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658034</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658034</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were euthanized by intraperitoneal injection of 20% urethane and the hypothalamus of mice was isolated and snap frozen in liquid nitrogen. RNA was isolated using RNAqueous (AM1914, Ambion) according to the manufacturer's protocol. Dynabeads mRNA DIRECT Micro Kit (Ambion) was used to isolate Intact mRNA. The total mRNA samples were depleted of up to 99.9% of 5S, 5.8S, 18S, and 28S rRNA using the RiboMinus Eukaryote System v2 (Life Technologies, Carlsbad, CA, USA). Barcoded cDNA libraries were constructed from the rRNA-depleted mRNA samples and prepared using the Ion Total-RNA Seq Kit v2 (Life Technologies).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17952595" alias="GSM6658035_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17952595</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658035_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658035: hypothalamus, WD, Tas1r3-/-, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA891954</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15469800">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15469800</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658035</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658035</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were euthanized by intraperitoneal injection of 20% urethane and the hypothalamus of mice was isolated and snap frozen in liquid nitrogen. RNA was isolated using RNAqueous (AM1914, Ambion) according to the manufacturer's protocol. Dynabeads mRNA DIRECT Micro Kit (Ambion) was used to isolate Intact mRNA. The total mRNA samples were depleted of up to 99.9% of 5S, 5.8S, 18S, and 28S rRNA using the RiboMinus Eukaryote System v2 (Life Technologies, Carlsbad, CA, USA). Barcoded cDNA libraries were constructed from the rRNA-depleted mRNA samples and prepared using the Ion Total-RNA Seq Kit v2 (Life Technologies).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17952596" alias="GSM6658036_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17952596</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658036_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658036: hypothalamus, WD, WT, rep1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA891954</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15469801">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15469801</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658036</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658036</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were euthanized by intraperitoneal injection of 20% urethane and the hypothalamus of mice was isolated and snap frozen in liquid nitrogen. RNA was isolated using RNAqueous (AM1914, Ambion) according to the manufacturer's protocol. Dynabeads mRNA DIRECT Micro Kit (Ambion) was used to isolate Intact mRNA. The total mRNA samples were depleted of up to 99.9% of 5S, 5.8S, 18S, and 28S rRNA using the RiboMinus Eukaryote System v2 (Life Technologies, Carlsbad, CA, USA). Barcoded cDNA libraries were constructed from the rRNA-depleted mRNA samples and prepared using the Ion Total-RNA Seq Kit v2 (Life Technologies).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX17952597" alias="GSM6658037_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX17952597</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6658037_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6658037: hypothalamus, WD, WT, rep2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP403423">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP403423</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA891954</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15469802">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15469802</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6658037</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6658037</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Mice were euthanized by intraperitoneal injection of 20% urethane and the hypothalamus of mice was isolated and snap frozen in liquid nitrogen. RNA was isolated using RNAqueous (AM1914, Ambion) according to the manufacturer's protocol. Dynabeads mRNA DIRECT Micro Kit (Ambion) was used to isolate Intact mRNA. The total mRNA samples were depleted of up to 99.9% of 5S, 5.8S, 18S, and 28S rRNA using the RiboMinus Eukaryote System v2 (Life Technologies, Carlsbad, CA, USA). Barcoded cDNA libraries were constructed from the rRNA-depleted mRNA samples and prepared using the Ion Total-RNA Seq Kit v2 (Life Technologies).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ION_TORRENT>
        <INSTRUMENT_MODEL>Ion Torrent Proton</INSTRUMENT_MODEL>
      </ION_TORRENT>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
