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        <LIBRARY_NAME>E8.0 Sox17^GFP/+ RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing definitive endodermal cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 8</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538432" alias="E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538432</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527825" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Insm1^GFP/GFP embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527825</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700091</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Insm1^GFP/GFP RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Insm1-lacking endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538433" alias="E-MTAB-2816:E8.0 Sox17 assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538433</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.0 Sox17 assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527826" refcenter="Vanderbilt University" refname="E-MTAB-2816:E8.0 Sox17^GFP/+ embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527826</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700092</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.0 Sox17^GFP/+ embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.0 Sox17^GFP/+ RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing definitive endodermal cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 8</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538434" alias="E-MTAB-2816:E9.5 Pdx1^CFP/+ assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538434</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Pdx1^CFP/+ assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527827" refcenter="Vanderbilt University" refname="E-MTAB-2816:E9.5 Pdx1^CFP/+  embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527827</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700093</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Pdx1^CFP/+  embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E9.5 Pdx1^CFP/+  RNA 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>See file RNA_extraction_protocol_for_FACS-isolated_cells.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>101</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Pdx1-expressing foregut endodermal cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 9.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538435" alias="E-MTAB-2816:E15.5 Ngn3^GFP/+ assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538435</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/+ assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527828" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Ngn3^GFP/+ embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527828</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700094</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/+ embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Ngn3^GFP/+ RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>neurogenin-3-expressing endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538436" alias="E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538436</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527829" refcenter="Vanderbilt University" refname="E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527829</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700095</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.5 Sox17^GFP/+ EpCAM+ RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing Epcam+ pancreatic epithelial cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 9.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538437" alias="E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538437</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
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        <IDENTIFIERS>
          <PRIMARY_ID>ERS527830</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700096</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Insm1^GFP/GFP RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Insm1-lacking endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
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    <IDENTIFIERS>
      <PRIMARY_ID>ERX538438</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E10.5 Ptf1a^YFP/+ assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527831" refcenter="Vanderbilt University" refname="E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527831</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700097</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E10.5 Ptf1a^YFP/+ RNA 1</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>See file RNA_extraction_protocol_for_FACS-isolated_cells.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Ptf1a-expressing multipotent pancreatic cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 10.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538439" alias="E-MTAB-2816:E15.5 Insm1^GFP/+ assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538439</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/+ assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527832" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Insm1^GFP/+ embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527832</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700098</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/+ embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Insm1^GFP/+ RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Insm1-expressing endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538440" alias="E-MTAB-2816:E8.5 Sox17 assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538440</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.5 Sox17 assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527833" refcenter="Vanderbilt University" refname="E-MTAB-2816:E8.5 Sox17^GFP/+ embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527833</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700099</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.5 Sox17^GFP/+ embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.5 Sox17^GFP/+ RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing definitive endodermal cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 8.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538441" alias="E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538441</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527834" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527834</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700100</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Ngn3^GFP/GFP RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>neurogenin-3-lacking pancreatic progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538442" alias="E-MTAB-2816:E15.5 Ngn3^GFP/+ assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538442</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/+ assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527835" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Ngn3^GFP/+ embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527835</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700101</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/+ embryos 2</SUBMITTER_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Ngn3^GFP/+ RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>neurogenin-3-expressing endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538443" alias="E-MTAB-2816:E8.5 Sox17 assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538443</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.5 Sox17 assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527836" refcenter="Vanderbilt University" refname="E-MTAB-2816:E8.5 Sox17^GFP/+ embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527836</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700102</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E8.5 Sox17^GFP/+ embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.5 Sox17^GFP/+ RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing definitive endodermal cell</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 8.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
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  <EXPERIMENT accession="ERX538444" alias="E-MTAB-2816:P60 MIP-GFP assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538444</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527837" refcenter="Vanderbilt University" refname="E-MTAB-2816:P60 MIP-GFP mice 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527837</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700103</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP mice 3</SUBMITTER_ID>
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      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P60 MIP-GFP RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
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        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>insulin-expressing mature beta cell</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>postnatal day 60</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538445" alias="E-MTAB-2816:E16.5 MIP-GFP assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538445</PRIMARY_ID>
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    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
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    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527838" refcenter="Vanderbilt University" refname="E-MTAB-2816:E16.5 MIP-GFP embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527838</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700104</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E16.5 MIP-GFP embryos 3</SUBMITTER_ID>
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      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E16.5 MIP-GFP RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>107</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
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        </SPOT_DECODE_SPEC>
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    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
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    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>insulin-expressing immature beta cell</VALUE>
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      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 16.5</VALUE>
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    </EXPERIMENT_ATTRIBUTES>
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      <PRIMARY_ID>ERX538446</PRIMARY_ID>
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    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
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      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
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    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527839" refcenter="Vanderbilt University" refname="E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527839</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700105</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E10.5 Ptf1a^YFP/+ RNA 2</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>See file RNA_extraction_protocol_for_FACS-isolated_cells.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Ptf1a-expressing multipotent pancreatic cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 10.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538447" alias="E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538447</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527840" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Insm1^GFP/GFP embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527840</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700106</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/GFP embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Insm1^GFP/GFP RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Insm1-lacking endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538448" alias="E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538448</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527841" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527841</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700107</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Ngn3^GFP/GFP RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>neurogenin-3-lacking pancreatic progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538449" alias="E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538449</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527842" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527842</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700108</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Ngn3^GFP/GFP embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Ngn3^GFP/GFP RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>neurogenin-3-lacking pancreatic progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538450" alias="E-MTAB-2816:P60 MIP-GFP assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538450</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527843" refcenter="Vanderbilt University" refname="E-MTAB-2816:P60 MIP-GFP mice 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527843</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700109</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP mice 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P60 MIP-GFP RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>insulin-expressing mature beta cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>postnatal day 60</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538451" alias="E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538451</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527844" refcenter="Vanderbilt University" refname="E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527844</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700110</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.5 Sox17^GFP/+ EpCAM+ RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing Epcam+ pancreatic epithelial cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 9.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538452" alias="E-MTAB-2816:E16.5 MIP-GFP assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538452</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E16.5 MIP-GFP assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527845" refcenter="Vanderbilt University" refname="E-MTAB-2816:E16.5 MIP-GFP embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527845</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700111</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E16.5 MIP-GFP embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E16.5 MIP-GFP RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>106</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>insulin-expressing immature beta cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 16.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538453" alias="E-MTAB-2816:E10.5 Ptf1a^YFP/+ assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538453</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E10.5 Ptf1a^YFP/+ assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527846" refcenter="Vanderbilt University" refname="E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527846</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700112</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E10.5 Ptf1a^YFP/+ embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E10.5 Ptf1a^YFP/+ RNA 3</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <SINGLE/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>See file RNA_extraction_protocol_for_FACS-isolated_cells.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Ptf1a-expressing multipotent pancreatic cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 10.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538454" alias="E-MTAB-2816:P60 MIP-GFP assay 1" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538454</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP assay 1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527847" refcenter="Vanderbilt University" refname="E-MTAB-2816:P60 MIP-GFP mice 1">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527847</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700113</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:P60 MIP-GFP mice 1</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>P60 MIP-GFP RNA 1</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>insulin-expressing mature beta cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>postnatal day 60</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538455" alias="E-MTAB-2816:E15.5 Insm1^GFP/+ assay 2" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538455</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/+ assay 2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527848" refcenter="Vanderbilt University" refname="E-MTAB-2816:E15.5 Insm1^GFP/+ embryos 2">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527848</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700114</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E15.5 Insm1^GFP/+ embryos 2</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E15.5 Insm1^GFP/+ RNA 2</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>111</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Insm1-expressing endocrine progenitor cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 15.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
  <EXPERIMENT accession="ERX538456" alias="E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 3" broker_name="ArrayExpress" center_name="Vanderbilt University">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX538456</PRIMARY_ID>
      <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17 EpCAM+ assay 3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 sequencing; Whole transcriptome profiling of beta cell development in the mouse</TITLE>
    <STUDY_REF accession="ERP006673" refcenter="Vanderbilt University" refname="E-MTAB-2816">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP006673</PRIMARY_ID>
        <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Whole transcriptome profiling of beta cell development in the mouse</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS527849" refcenter="Vanderbilt University" refname="E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 3">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS527849</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA2700115</EXTERNAL_ID>
          <SUBMITTER_ID namespace="Vanderbilt University">E-MTAB-2816:E9.5 Sox17^GFP/+ embryos 3</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>E8.5 Sox17^GFP/+ EpCAM+ RNA 3</LIBRARY_NAME>
        <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 isolated using TRIzol LS (Invitrogen) and column purification (Zymo Research), according to manufacturers instructions. RNA was DNase-treated (Ambion) and integrity was assessed on the Bioanalyzer (Agilent). See file RNA_extraction_for_FACS.doc. As per manufacturer instructions. The library was constructed using the Illumina TruSeq DNA sample prep kits A&amp;B, FC-121-1001 and FC-121-1002 with the standard Illumina methods (Bentley 2008).</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
      <SPOT_DESCRIPTOR>
        <SPOT_DECODE_SPEC>
          <SPOT_LENGTH>110</SPOT_LENGTH>
          <READ_SPEC>
            <READ_INDEX>0</READ_INDEX>
            <READ_CLASS>Application Read</READ_CLASS>
            <READ_TYPE>Forward</READ_TYPE>
            <BASE_COORD>1</BASE_COORD>
          </READ_SPEC>
        </SPOT_DECODE_SPEC>
      </SPOT_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
    <EXPERIMENT_ATTRIBUTES>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: cell type</TAG>
        <VALUE>Sox17-expressing Epcam+ pancreatic epithelial cell</VALUE>
      </EXPERIMENT_ATTRIBUTE>
      <EXPERIMENT_ATTRIBUTE>
        <TAG>Experimental Factor: developmental stage</TAG>
        <VALUE>embryonic day 9.5</VALUE>
      </EXPERIMENT_ATTRIBUTE>
    </EXPERIMENT_ATTRIBUTES>
  </EXPERIMENT>
</EXPERIMENT_SET>
