<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18303723" alias="GSM6738592_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303723</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738592_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738592: V16D_siControl_1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794464</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738592</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738592</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303724" alias="GSM6738593_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303724</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738593_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738593: V16D_siControl_2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794465</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738593</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738593</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303725" alias="GSM6738594_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303725</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738594_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738594: V16D_siControl_3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794466</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738594</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738594</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303726" alias="GSM6738595_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303726</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738595_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738595: V16D_siControl_4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794467</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738595</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738595</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303727" alias="GSM6738596_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303727</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738596_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738596: V16D_siControl_5; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794468</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738596</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738596</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303728" alias="GSM6738597_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303728</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738597_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738597: V16D_siControl_6; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794469</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738597</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738597</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303729" alias="GSM6738598_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303729</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738598_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738598: V16D_siDECR2_1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794470</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738598</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738598</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303730" alias="GSM6738599_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303730</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738599_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738599: V16D_siDECR2_2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794471</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738599</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738599</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303731" alias="GSM6738600_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303731</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738600_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738600: V16D_siDECR2_3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794472</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738600</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738600</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303732" alias="GSM6738601_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303732</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738601_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738601: V16D_siDECR2_4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794473">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794473</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738601</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738601</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303733" alias="GSM6738602_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303733</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738602_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738602: V16D_siDECR2_5; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738602</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738602</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303734" alias="GSM6738603_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303734</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738603_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738603: V16D_siDECR2_6; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738603</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738603</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303735" alias="GSM6738604_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303735</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738604_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738604: MR49F_siControl_1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738604</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738604</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303736" alias="GSM6738605_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303736</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738605_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738605: MR49F_siControl_2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738605</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738605</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303737" alias="GSM6738606_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303737</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738606_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738606: MR49F_siControl_3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738606</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738606</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303738" alias="GSM6738607_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303738</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738607_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738607: MR49F_siControl_4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738607</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738607</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303739" alias="GSM6738608_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303739</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738608_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738608: MR49F_siControl_5; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738608</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738608</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303740" alias="GSM6738609_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303740</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738609_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738609: MR49F_siControl_6; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738609</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738609</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303741" alias="GSM6738610_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303741</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738610_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738610: MR49F_siDECR2_1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738610</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738610</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303742" alias="GSM6738611_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303742</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738611_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738611: MR49F_siDECR2_2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794483</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738611</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738611</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303743" alias="GSM6738612_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303743</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738612_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738612: MR49F_siDECR2_3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794484</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738612</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738612</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303744" alias="GSM6738613_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303744</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738613_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738613: MR49F_siDECR2_4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794485">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794485</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738613</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738613</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303745" alias="GSM6738614_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303745</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738614_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738614: MR49F_siDECR2_5; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794486">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794486</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738614</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738614</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18303746" alias="GSM6738615_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18303746</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6738615_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6738615: MR49F_siDECR2_6; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP408556">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP408556</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA903079</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS15794487">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS15794487</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6738615</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6738615</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 RNA was extracted using Trizol and the RNeasy Micro Kit (Qiagen), according to the manufacturer's instructions. Stranded polyA libraries were generated using the Nugen Universal Plus mRNA-seq protocol (M01442 v2) and converted to MGI compatible libraries using the MGIEasy Universal Library Conversion Kit. RNA-seq; MGI DNBSEQ G400 (paired-end, 2 x 98bp)</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <DNBSEQ>
        <INSTRUMENT_MODEL>DNBSEQ-G400</INSTRUMENT_MODEL>
      </DNBSEQ>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
