<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX18538042" alias="GSM6805960_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538042</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805960_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805960: SF3B1 MUT t0, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002458">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002458</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805960</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805960</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538043" alias="GSM6805961_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538043</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805961_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805961: SF3B1 MUT t0, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002459">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002459</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805961</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805961</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538044" alias="GSM6805962_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538044</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805962_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805962: SF3B1 MUT t0, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002460">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002460</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805962</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805962</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538045" alias="GSM6805963_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538045</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805963_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805963: SF3B1 MUT t24, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002461">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002461</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805963</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805963</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538046" alias="GSM6805964_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538046</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805964_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805964: SF3B1 MUT t24, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002462">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002462</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805964</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805964</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538047" alias="GSM6805965_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538047</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805965_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805965: SF3B1 MUT t24, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002463">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002463</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805965</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805965</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538048" alias="GSM6805966_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538048</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805966_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805966: SF3B1 WT t0, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002464">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002464</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805966</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805966</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538049" alias="GSM6805967_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538049</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805967_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805967: SF3B1 WT t0, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002465">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002465</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805967</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805967</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538050" alias="GSM6805968_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538050</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805968_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805968: SF3B1 WT t0, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002466">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002466</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805968</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805968</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538051" alias="GSM6805969_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538051</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805969_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805969: SF3B1 WT t24, rep 1; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002467</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805969</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805969</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538052" alias="GSM6805970_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538052</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805970_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805970: SF3B1 WT t24, rep 2; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002468</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805970</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805970</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX18538053" alias="GSM6805971_r1">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX18538053</PRIMARY_ID>
      <EXTERNAL_ID namespace="GEO">GSM6805971_r1</EXTERNAL_ID>
    </IDENTIFIERS>
    <TITLE>GSM6805971: SF3B1 WT t24, rep 3; Mus musculus; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP411997">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP411997</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA910113</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS16002469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS16002469</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM6805971</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GSM6805971</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Samples were controled with an Agilent 2100 Bioanalyzer. RNA polyA was realized with the NEBNext polyA kit + Ultra II &lt; 150ng. Libraries were constructed using the TruSeq Stranded mRNA Sample Preparation Kit (Illumina, San Diego, CA), &gt; 150ng BA-mRNA. Bank were normalized and controled with a Bioanalyzer.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>NextSeq 500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
