<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM2871734" accession="SRX3436519">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436519</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871734</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871734: R1_TamR_NS_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727467">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727467</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871734</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871734</ID>
          <LABEL>GSM2871734</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871734</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871735" accession="SRX3436520">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436520</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871735</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871735: R1_TamR_NS_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727468">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727468</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871735</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871735</ID>
          <LABEL>GSM2871735</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871735</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871736" accession="SRX3436521">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436521</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871736</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871736: R1_TamR_NS_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727469">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727469</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871736</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871736</ID>
          <LABEL>GSM2871736</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871736</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871737" accession="SRX3436522">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436522</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871737</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871737: R1_TamR_4E_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727470">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727470</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871737</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871737</ID>
          <LABEL>GSM2871737</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871737</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871738" accession="SRX3436523">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436523</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871738</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871738: R1_TamR_4E_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727471">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727471</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871738</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871738</ID>
          <LABEL>GSM2871738</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871738</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871739" accession="SRX3436524">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436524</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871739</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871739: R1_TamR_4E_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727511">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727511</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871739</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871739</ID>
          <LABEL>GSM2871739</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871739</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871740" accession="SRX3436525">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436525</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871740</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871740: R1_TamS_NS_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727472">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727472</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871740</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871740</ID>
          <LABEL>GSM2871740</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871740</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871741" accession="SRX3436526">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436526</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871741</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871741: R1_TamS_NS_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727474">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727474</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871741</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871741</ID>
          <LABEL>GSM2871741</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871741</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871742" accession="SRX3436527">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436527</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871742</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871742: R1_TamS_NS_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727475">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727475</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871742</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871742</ID>
          <LABEL>GSM2871742</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871742</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871743" accession="SRX3436528">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436528</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871743</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871743: R2_TamR_NS_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727477">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727477</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871743</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871743</ID>
          <LABEL>GSM2871743</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871743</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871744" accession="SRX3436529">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436529</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871744</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871744: R2_TamR_NS_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727476">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727476</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871744</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871744</ID>
          <LABEL>GSM2871744</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871744</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871745" accession="SRX3436530">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436530</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871745</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871745: R2_TamR_NS_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727478">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727478</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871745</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871745</ID>
          <LABEL>GSM2871745</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871745</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871746" accession="SRX3436531">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436531</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871746</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871746: R2_TamR_4E_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727479">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727479</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871746</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871746</ID>
          <LABEL>GSM2871746</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871746</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871747" accession="SRX3436532">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436532</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871747</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871747: R2_TamR_4E_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727480">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727480</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871747</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871747</ID>
          <LABEL>GSM2871747</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871747</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871748" accession="SRX3436533">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436533</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871748</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871748: R2_TamR_4E_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727481">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727481</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871748</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871748</ID>
          <LABEL>GSM2871748</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871748</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871749" accession="SRX3436534">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436534</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871749</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871749: R2_TamS_NS_HD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727482">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727482</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871749</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871749</ID>
          <LABEL>GSM2871749</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871749</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871750" accession="SRX3436535">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436535</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871750</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871750: R2_TamS_NS_LD; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727483">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727483</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871750</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871750</ID>
          <LABEL>GSM2871750</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871750</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM2871751" accession="SRX3436536">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX3436536</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM2871751</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM2871751: R2_TamS_NS_T; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP125951" refname="GSE107590">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP125951</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS2727484">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2727484</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM2871751</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>Lysates were either purified (total mRNA) or subjected to polysome profiling.  Polysome profiling samples pertaining to 2-3 ribsomes (light mRNA) were purified or &gt;4 ribosomes were purified (heavy mRNA).  All samples were purified using the RNeasy Mini Kit (Qiagen) as per manufacture instructions. RNA libraries were prepared for sequencing using poly A enrichment standard Illumina protocols</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>302871751</ID>
          <LABEL>GSM2871751</LABEL>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM2871751</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
