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      <SAMPLE_DESCRIPTOR accession="SRS711012">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711012</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514009</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514009</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514009</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514009</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514009</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514010" accession="SRX712887" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712887</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514010</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514010: RNA-seq siCont ActD 2h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711013">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711013</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514010</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514010</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514010</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514010</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514010</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514011" accession="SRX712888" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712888</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514011</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514011: RNA-seq siCont ActD 4h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711014">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711014</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514011</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514011</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514011</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514011</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514011</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514012" accession="SRX712889" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712889</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514012</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514012: RNA-seq siTUT47 ActD 0h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711015">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711015</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514012</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514012</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514012</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514012</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514012</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514013" accession="SRX712890" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712890</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514013</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514013: RNA-seq siTUT47 ActD 1h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711017">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711017</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514013</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514013</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514013</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514013</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514013</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514014" accession="SRX712891" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712891</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514014</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514014: RNA-seq siTUT47 ActD 2h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711016">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711016</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514014</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514014</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514014</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514014</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514014</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1514015" accession="SRX712892" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX712892</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1514015</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1514015: RNA-seq siTUT47 ActD 4h (biological replicate #2); Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP044679" refname="GSE59626">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP044679</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS711018">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS711018</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1514015</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>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Total RNAs were extracted by TRIzol (Invitrogen), and the quality was checked by  Bioanalyzer 2100 (Agilent). The same amount of control poly(A) spike-in (Affymetrix,  #900433) was mixed with each sample with the same amount of total RNA, and  subsequently rRNA was depleted by Ribo-Zero (Epicentre). RNA-seq libraries were  constructed using Illumina TruSeq RNA sample preparation kit v2.</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1514015</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1514015</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301514015</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1514015</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
