<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="GSM1550090" accession="SRX763494" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763494</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550090</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550090: H1047R 12hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747951">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747951</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550090</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550090</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550090</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550090</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550090</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550091" accession="SRX763495" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763495</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550091</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550091: H1047R 12hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747952">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747952</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550091</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550091</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550091</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550091</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550091</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550092" accession="SRX763496" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763496</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550092</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550092: H1047R 12hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747953">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747953</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550092</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550092</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550092</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550092</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550092</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550093" accession="SRX763497" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763497</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550093</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550093: H1047R 24hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747954">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747954</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550093</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550093</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550093</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550093</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550093</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550094" accession="SRX763498" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763498</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550094</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550094: H1047R 24hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747955">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747955</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550094</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550094</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550094</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550094</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550094</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550095" accession="SRX763499" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763499</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550095</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550095: H1047R 24hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747956">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747956</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550095</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550095</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550095</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550095</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550095</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550096" accession="SRX763500" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763500</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550096</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550096: H1047R 6hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747957">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747957</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550096</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550096</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550096</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550096</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550096</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550097" accession="SRX763501" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763501</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550097</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550097: H1047R 6hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747958">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747958</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550097</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550097</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550097</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550097</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550097</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550098" accession="SRX763502" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763502</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550098</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550098: H1047R 6hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747959">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747959</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550098</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550098</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550098</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550098</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550098</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550099" accession="SRX763503" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763503</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550099</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550099: WT 6hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747960">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747960</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550099</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550099</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550099</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550099</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550099</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550100" accession="SRX763504" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763504</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550100</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550100: WT 6hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747961">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747961</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550100</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550100</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550100</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550100</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550100</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550101" accession="SRX763505" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763505</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550101</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550101: WT 6hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747962">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747962</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550101</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550101</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550101</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550101</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550101</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550102" accession="SRX763506" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763506</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550102</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550102: WT 6hr rep4; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747963">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747963</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550102</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550102</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550102</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550102</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550102</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550103" accession="SRX763507" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763507</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550103</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550103: H1047R 0hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747964">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747964</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550103</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550103</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550103</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550103</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550103</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550104" accession="SRX763508" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763508</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550104</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550104: H1047R 0hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747965">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747965</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550104</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550104</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550104</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550104</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550104</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550105" accession="SRX763509" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763509</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550105</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550105: H1047R 0hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747966">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747966</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550105</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550105</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550105</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550105</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550105</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550106" accession="SRX763510" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763510</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550106</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550106: WT 0hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747967">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747967</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550106</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550106</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550106</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550106</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550106</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550107" accession="SRX763511" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763511</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550107</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550107: WT 0hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747968">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747968</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550107</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550107</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550107</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550107</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550107</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550108" accession="SRX763512" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763512</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550108</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550108: WT 0hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747969">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747969</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550108</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550108</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550108</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550108</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550108</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550109" accession="SRX763513" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763513</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550109</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550109: WT 12hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747970">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747970</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550109</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550109</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550109</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550109</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550109</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550110" accession="SRX763514" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763514</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550110</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550110: WT 12hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747971">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747971</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550110</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550110</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550110</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550110</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550110</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550111" accession="SRX763515" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763515</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550111</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550111: WT 12hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747972">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747972</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550111</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550111</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550111</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550111</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550111</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550112" accession="SRX763516" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763516</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550112</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550112: WT 24hr rep1; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747973">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747973</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550112</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550112</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550112</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550112</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550112</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550113" accession="SRX763517" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763517</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550113</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550113: WT 24hr rep2; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747974">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747974</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550113</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550113</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550113</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550113</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550113</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT alias="GSM1550114" accession="SRX763518" center_name="GEO">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX763518</PRIMARY_ID>
      <SUBMITTER_ID namespace="GEO">GSM1550114</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>GSM1550114: WT 24hr rep3; Homo sapiens; RNA-Seq</TITLE>
    <STUDY_REF accession="SRP050036" refname="GSE63452">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP050036</PRIMARY_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION/>
      <SAMPLE_DESCRIPTOR accession="SRS747975">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS747975</PRIMARY_ID>
          <EXTERNAL_ID namespace="GEO">GSM1550114</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 RNA was extracted using Trizol following standard protocol.  1mL Trizol was added directly to cells, RNA was separated from protein and DNA using 200uL chloroform.  Aqueous layer was removed and total RNA was precipitated using 500uL isopropanol precipitation.    This precipitate was redissolved and precipitated with 250uL DEPC treated water folled by 750uL anhydrous ethanol.  Pellet was redissolved in 200uL DEPC treated water. Residual DNA was eliminated using Ambion Dneasy kits. Nugen Ovation protocol</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_LINKS>
      <EXPERIMENT_LINK>
        <URL_LINK>
          <LABEL>GEO Sample GSM1550114</LABEL>
          <URL>http://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSM1550114</URL>
        </URL_LINK>
      </EXPERIMENT_LINK>
      <EXPERIMENT_LINK>
        <XREF_LINK>
          <DB>gds</DB>
          <ID>301550114</ID>
        </XREF_LINK>
      </EXPERIMENT_LINK>
    </EXPERIMENT_LINKS>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>GEO Accession</TAG>
        <VALUE>GSM1550114</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
