<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="SC_EXP_13329_1#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX941344">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941344</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597896, constructed from sample accession ERS700353 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGATAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700353" refname="RNA_140619_A1-sc-1996883" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700353</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A1-sc-1996883</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597896</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX941345">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941345</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597897, constructed from sample accession ERS700354 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700354" refname="RNA_140619_A2-sc-1996884" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700354</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A2-sc-1996884</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597897</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX941346">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941346</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597898, constructed from sample accession ERS700355 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAATAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700355" refname="RNA_140619_A3-sc-1996885" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700355</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A3-sc-1996885</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597898</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX941347">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941347</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597899, constructed from sample accession ERS700356 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700356" refname="RNA_140619_A4-sc-1996886" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700356</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A4-sc-1996886</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597899</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX941348">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941348</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597900, constructed from sample accession ERS700357 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700357" refname="RNA_140619_A5-sc-1996887" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700357</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A5-sc-1996887</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597900</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX941349">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941349</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597902, constructed from sample accession ERS700358 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700358" refname="RNA_140619_A7-sc-1996889" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700358</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A7-sc-1996889</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597902</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX941350">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941350</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597903, constructed from sample accession ERS700359 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700359" refname="RNA_140619_A8-sc-1996890" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700359</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A8-sc-1996890</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597903</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX941351">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941351</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597906, constructed from sample accession ERS700360 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGACTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700360" refname="RNA_140619_B1-sc-1996893" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700360</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B1-sc-1996893</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597906</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX941352">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941352</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597907, constructed from sample accession ERS700361 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700361" refname="RNA_140619_B2-sc-1996894" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700361</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B2-sc-1996894</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX941353">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941353</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597908, constructed from sample accession ERS700362 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAACTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700362" refname="RNA_140619_B3-sc-1996895" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700362</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B3-sc-1996895</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX941354">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941354</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597909, constructed from sample accession ERS700363 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700363" refname="RNA_140619_B4-sc-1996896" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700363</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B4-sc-1996896</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX941355">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941355</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597910, constructed from sample accession ERS700364 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700364" refname="RNA_140619_B5-sc-1996897" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700364</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B5-sc-1996897</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX941356">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941356</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597912, constructed from sample accession ERS700365 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700365" refname="RNA_140619_B7-sc-1996899" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700365</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B7-sc-1996899</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX941357">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941357</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597913, constructed from sample accession ERS700366 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700366" refname="RNA_140619_B8-sc-1996900" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700366</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B8-sc-1996900</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX941358">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941358</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597916, constructed from sample accession ERS700367 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGATATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700367" refname="RNA_140619_C1-sc-1996903" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700367</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C1-sc-1996903</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX941359">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941359</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597917, constructed from sample accession ERS700368 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700368" refname="RNA_140619_C2-sc-1996904" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700368</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C2-sc-1996904</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX941360">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941360</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597918, constructed from sample accession ERS700369 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAATATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700369" refname="RNA_140619_C3-sc-1996905" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700369</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C3-sc-1996905</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX941361">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941361</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597919, constructed from sample accession ERS700370 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700370" refname="RNA_140619_C4-sc-1996906" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700370</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C4-sc-1996906</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX941362">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941362</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597920, constructed from sample accession ERS700371 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700371" refname="RNA_140619_C5-sc-1996907" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700371</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C5-sc-1996907</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX941363">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941363</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597922, constructed from sample accession ERS700372 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700372" refname="RNA_140619_C7-sc-1996909" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700372</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C7-sc-1996909</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX941364">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941364</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597923, constructed from sample accession ERS700373 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700373" refname="RNA_140619_C8-sc-1996910" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700373</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C8-sc-1996910</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX941365">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941365</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597926, constructed from sample accession ERS700374 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGAAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700374" refname="RNA_140619_D1-sc-1996913" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700374</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D1-sc-1996913</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX941366">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941366</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597927, constructed from sample accession ERS700375 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700375" refname="RNA_140619_D2-sc-1996914" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700375</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D2-sc-1996914</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX941367">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941367</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597928, constructed from sample accession ERS700376 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAAAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700376" refname="RNA_140619_D3-sc-1996915" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700376</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D3-sc-1996915</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX941368">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941368</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597929, constructed from sample accession ERS700377 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700377" refname="RNA_140619_D4-sc-1996916" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700377</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D4-sc-1996916</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX941369">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941369</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597930, constructed from sample accession ERS700378 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700378" refname="RNA_140619_D5-sc-1996917" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700378</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D5-sc-1996917</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX941370">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941370</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597932, constructed from sample accession ERS700379 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700379" refname="RNA_140619_D7-sc-1996919" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700379</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D7-sc-1996919</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX941371">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941371</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597933, constructed from sample accession ERS700380 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700380" refname="RNA_140619_D8-sc-1996920" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700380</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D8-sc-1996920</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX941372">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941372</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597936, constructed from sample accession ERS700381 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGAGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700381" refname="RNA_140619_E1-sc-1996923" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700381</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E1-sc-1996923</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX941373">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941373</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597937, constructed from sample accession ERS700382 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700382" refname="RNA_140619_E2-sc-1996924" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700382</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E2-sc-1996924</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX941374">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941374</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597938, constructed from sample accession ERS700383 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAAGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700383" refname="RNA_140619_E3-sc-1996925" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700383</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E3-sc-1996925</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX941375">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941375</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597939, constructed from sample accession ERS700384 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700384" refname="RNA_140619_E4-sc-1996926" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700384</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E4-sc-1996926</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX941376">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941376</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597940, constructed from sample accession ERS700385 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700385" refname="RNA_140619_E5-sc-1996927" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700385</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E5-sc-1996927</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX941377">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941377</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597942, constructed from sample accession ERS700386 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700386" refname="RNA_140619_E7-sc-1996929" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700386</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E7-sc-1996929</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX941378">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941378</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597943, constructed from sample accession ERS700387 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700387" refname="RNA_140619_E8-sc-1996930" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700387</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E8-sc-1996930</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX941379">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941379</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597946, constructed from sample accession ERS700388 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGAACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700388" refname="RNA_140619_F1-sc-1996933" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700388</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F1-sc-1996933</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX941380">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941380</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597947, constructed from sample accession ERS700389 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700389" refname="RNA_140619_F2-sc-1996934" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700389</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F2-sc-1996934</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX941381">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941381</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597948, constructed from sample accession ERS700390 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAAACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700390" refname="RNA_140619_F3-sc-1996935" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700390</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F3-sc-1996935</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX941382">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941382</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597949, constructed from sample accession ERS700391 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700391" refname="RNA_140619_F4-sc-1996936" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700391</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F4-sc-1996936</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX941383">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941383</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597950, constructed from sample accession ERS700392 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700392" refname="RNA_140619_F5-sc-1996937" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700392</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F5-sc-1996937</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX941384">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941384</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597952, constructed from sample accession ERS700393 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700393" refname="RNA_140619_F7-sc-1996939" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700393</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F7-sc-1996939</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX941385">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941385</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597953, constructed from sample accession ERS700394 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700394" refname="RNA_140619_F8-sc-1996940" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700394</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F8-sc-1996940</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX941386">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941386</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597956, constructed from sample accession ERS700395 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGAAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700395" refname="RNA_140619_G1-sc-1996943" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700395</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G1-sc-1996943</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597956</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX941387">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941387</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597957, constructed from sample accession ERS700396 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700396" refname="RNA_140619_G2-sc-1996944" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700396</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G2-sc-1996944</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597957</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX941388">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941388</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597958, constructed from sample accession ERS700397 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAAAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700397" refname="RNA_140619_G3-sc-1996945" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700397</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G3-sc-1996945</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597958</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX941389">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941389</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597959, constructed from sample accession ERS700398 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700398" refname="RNA_140619_G4-sc-1996946" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700398</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G4-sc-1996946</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597959</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX941390">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941390</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597960, constructed from sample accession ERS700399 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700399" refname="RNA_140619_G5-sc-1996947" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700399</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G5-sc-1996947</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597960</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX941391">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941391</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597962, constructed from sample accession ERS700400 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700400" refname="RNA_140619_G7-sc-1996949" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700400</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G7-sc-1996949</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597962</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX941392">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941392</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597963, constructed from sample accession ERS700401 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700401" refname="RNA_140619_G8-sc-1996950" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700401</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G8-sc-1996950</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597963</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX941393">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941393</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597966, constructed from sample accession ERS700402 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TAAGGCGACTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700402" refname="RNA_140619_H1-sc-1996953" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700402</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H1-sc-1996953</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597966</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX941394">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941394</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597967, constructed from sample accession ERS700403 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CGTACTAGCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700403" refname="RNA_140619_H2-sc-1996954" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700403</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H2-sc-1996954</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597967</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX941395">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941395</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597968, constructed from sample accession ERS700404 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence AGGCAGAACTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700404" refname="RNA_140619_H3-sc-1996955" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700404</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H3-sc-1996955</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597968</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX941396">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941396</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597969, constructed from sample accession ERS700405 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence TCCTGAGCCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700405" refname="RNA_140619_H4-sc-1996956" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700405</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H4-sc-1996956</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597969</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX941397">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941397</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597970, constructed from sample accession ERS700406 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence GGACTCCTCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700406" refname="RNA_140619_H5-sc-1996957" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700406</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H5-sc-1996957</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597970</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX941398">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941398</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597972, constructed from sample accession ERS700407 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CTCTCTACCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700407" refname="RNA_140619_H7-sc-1996959" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700407</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H7-sc-1996959</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597972</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_1#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX941399">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941399</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_1#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_1#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597973, constructed from sample accession ERS700408 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_1).  This submission includes reads tagged with the sequence CAGAGAGGCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700408" refname="RNA_140619_H8-sc-1996960" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700408</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H8-sc-1996960</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597973</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#1" center_name="The Wellcome Trust Sanger Institute" accession="ERX941400">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941400</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#1</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#1</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597896, constructed from sample accession ERS700353 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGATAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700353" refname="RNA_140619_A1-sc-1996883" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700353</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A1-sc-1996883</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597896</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#2" center_name="The Wellcome Trust Sanger Institute" accession="ERX941401">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941401</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#2</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#2</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597897, constructed from sample accession ERS700354 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700354" refname="RNA_140619_A2-sc-1996884" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700354</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A2-sc-1996884</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597897</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#3" center_name="The Wellcome Trust Sanger Institute" accession="ERX941402">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941402</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#3</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#3</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597898, constructed from sample accession ERS700355 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAATAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700355" refname="RNA_140619_A3-sc-1996885" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700355</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A3-sc-1996885</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597898</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#4" center_name="The Wellcome Trust Sanger Institute" accession="ERX941403">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941403</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#4</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#4</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597899, constructed from sample accession ERS700356 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700356" refname="RNA_140619_A4-sc-1996886" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700356</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A4-sc-1996886</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597899</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#5" center_name="The Wellcome Trust Sanger Institute" accession="ERX941404">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941404</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#5</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#5</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597900, constructed from sample accession ERS700357 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700357" refname="RNA_140619_A5-sc-1996887" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700357</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A5-sc-1996887</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597900</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#7" center_name="The Wellcome Trust Sanger Institute" accession="ERX941405">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941405</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#7</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#7</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597902, constructed from sample accession ERS700358 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700358" refname="RNA_140619_A7-sc-1996889" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700358</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A7-sc-1996889</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597902</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#8" center_name="The Wellcome Trust Sanger Institute" accession="ERX941406">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941406</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#8</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#8</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597903, constructed from sample accession ERS700359 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGTAGATCGC.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700359" refname="RNA_140619_A8-sc-1996890" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700359</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_A8-sc-1996890</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597903</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#13" center_name="The Wellcome Trust Sanger Institute" accession="ERX941407">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941407</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#13</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#13</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597906, constructed from sample accession ERS700360 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGACTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700360" refname="RNA_140619_B1-sc-1996893" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700360</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B1-sc-1996893</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597906</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#14" center_name="The Wellcome Trust Sanger Institute" accession="ERX941408">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941408</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#14</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#14</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597907, constructed from sample accession ERS700361 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700361" refname="RNA_140619_B2-sc-1996894" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700361</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B2-sc-1996894</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597907</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#15" center_name="The Wellcome Trust Sanger Institute" accession="ERX941409">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941409</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#15</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#15</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597908, constructed from sample accession ERS700362 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAACTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700362" refname="RNA_140619_B3-sc-1996895" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700362</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B3-sc-1996895</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597908</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#16" center_name="The Wellcome Trust Sanger Institute" accession="ERX941410">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941410</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#16</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#16</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597909, constructed from sample accession ERS700363 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700363" refname="RNA_140619_B4-sc-1996896" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700363</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B4-sc-1996896</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597909</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#17" center_name="The Wellcome Trust Sanger Institute" accession="ERX941411">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941411</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#17</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#17</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597910, constructed from sample accession ERS700364 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700364" refname="RNA_140619_B5-sc-1996897" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700364</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B5-sc-1996897</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597910</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#19" center_name="The Wellcome Trust Sanger Institute" accession="ERX941412">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941412</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#19</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#19</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597912, constructed from sample accession ERS700365 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700365" refname="RNA_140619_B7-sc-1996899" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700365</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B7-sc-1996899</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597912</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#20" center_name="The Wellcome Trust Sanger Institute" accession="ERX941413">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941413</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#20</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#20</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597913, constructed from sample accession ERS700366 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGCTCTCTAT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700366" refname="RNA_140619_B8-sc-1996900" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700366</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_B8-sc-1996900</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597913</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#25" center_name="The Wellcome Trust Sanger Institute" accession="ERX941414">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941414</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#25</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#25</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597916, constructed from sample accession ERS700367 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGATATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700367" refname="RNA_140619_C1-sc-1996903" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700367</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C1-sc-1996903</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597916</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#26" center_name="The Wellcome Trust Sanger Institute" accession="ERX941415">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941415</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#26</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#26</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597917, constructed from sample accession ERS700368 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700368" refname="RNA_140619_C2-sc-1996904" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700368</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C2-sc-1996904</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597917</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#27" center_name="The Wellcome Trust Sanger Institute" accession="ERX941416">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941416</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#27</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#27</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597918, constructed from sample accession ERS700369 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAATATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700369" refname="RNA_140619_C3-sc-1996905" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700369</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C3-sc-1996905</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597918</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#28" center_name="The Wellcome Trust Sanger Institute" accession="ERX941417">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941417</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#28</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#28</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597919, constructed from sample accession ERS700370 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700370" refname="RNA_140619_C4-sc-1996906" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700370</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C4-sc-1996906</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597919</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#29" center_name="The Wellcome Trust Sanger Institute" accession="ERX941418">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941418</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#29</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#29</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597920, constructed from sample accession ERS700371 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700371" refname="RNA_140619_C5-sc-1996907" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700371</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C5-sc-1996907</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597920</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#31" center_name="The Wellcome Trust Sanger Institute" accession="ERX941419">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941419</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#31</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#31</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597922, constructed from sample accession ERS700372 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700372" refname="RNA_140619_C7-sc-1996909" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700372</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C7-sc-1996909</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597922</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#32" center_name="The Wellcome Trust Sanger Institute" accession="ERX941420">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941420</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#32</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#32</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597923, constructed from sample accession ERS700373 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGTATCCTCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700373" refname="RNA_140619_C8-sc-1996910" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700373</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_C8-sc-1996910</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597923</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#37" center_name="The Wellcome Trust Sanger Institute" accession="ERX941421">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941421</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#37</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#37</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597926, constructed from sample accession ERS700374 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGAAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700374" refname="RNA_140619_D1-sc-1996913" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700374</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D1-sc-1996913</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597926</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#38" center_name="The Wellcome Trust Sanger Institute" accession="ERX941422">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941422</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#38</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#38</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597927, constructed from sample accession ERS700375 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700375" refname="RNA_140619_D2-sc-1996914" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700375</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D2-sc-1996914</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597927</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#39" center_name="The Wellcome Trust Sanger Institute" accession="ERX941423">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941423</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#39</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#39</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597928, constructed from sample accession ERS700376 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAAAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700376" refname="RNA_140619_D3-sc-1996915" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700376</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D3-sc-1996915</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597928</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#40" center_name="The Wellcome Trust Sanger Institute" accession="ERX941424">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941424</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#40</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#40</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597929, constructed from sample accession ERS700377 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700377" refname="RNA_140619_D4-sc-1996916" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700377</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D4-sc-1996916</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597929</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#41" center_name="The Wellcome Trust Sanger Institute" accession="ERX941425">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941425</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#41</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#41</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597930, constructed from sample accession ERS700378 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700378" refname="RNA_140619_D5-sc-1996917" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700378</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D5-sc-1996917</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597930</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#43" center_name="The Wellcome Trust Sanger Institute" accession="ERX941426">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941426</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#43</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#43</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597932, constructed from sample accession ERS700379 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700379" refname="RNA_140619_D7-sc-1996919" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700379</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D7-sc-1996919</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597932</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#44" center_name="The Wellcome Trust Sanger Institute" accession="ERX941427">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941427</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#44</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#44</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597933, constructed from sample accession ERS700380 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGAGAGTAGA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700380" refname="RNA_140619_D8-sc-1996920" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700380</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_D8-sc-1996920</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597933</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#49" center_name="The Wellcome Trust Sanger Institute" accession="ERX941428">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941428</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#49</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#49</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597936, constructed from sample accession ERS700381 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGAGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700381" refname="RNA_140619_E1-sc-1996923" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700381</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E1-sc-1996923</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597936</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#50" center_name="The Wellcome Trust Sanger Institute" accession="ERX941429">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941429</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#50</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#50</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597937, constructed from sample accession ERS700382 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700382" refname="RNA_140619_E2-sc-1996924" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700382</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E2-sc-1996924</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597937</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#51" center_name="The Wellcome Trust Sanger Institute" accession="ERX941430">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941430</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#51</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#51</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597938, constructed from sample accession ERS700383 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAAGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700383" refname="RNA_140619_E3-sc-1996925" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700383</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E3-sc-1996925</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597938</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#52" center_name="The Wellcome Trust Sanger Institute" accession="ERX941431">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941431</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#52</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#52</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597939, constructed from sample accession ERS700384 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700384" refname="RNA_140619_E4-sc-1996926" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700384</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E4-sc-1996926</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597939</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#53" center_name="The Wellcome Trust Sanger Institute" accession="ERX941432">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941432</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#53</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#53</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597940, constructed from sample accession ERS700385 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700385" refname="RNA_140619_E5-sc-1996927" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700385</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E5-sc-1996927</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597940</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#55" center_name="The Wellcome Trust Sanger Institute" accession="ERX941433">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941433</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#55</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#55</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597942, constructed from sample accession ERS700386 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700386" refname="RNA_140619_E7-sc-1996929" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700386</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E7-sc-1996929</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597942</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#56" center_name="The Wellcome Trust Sanger Institute" accession="ERX941434">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941434</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#56</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#56</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597943, constructed from sample accession ERS700387 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGGTAAGGAG.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700387" refname="RNA_140619_E8-sc-1996930" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700387</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_E8-sc-1996930</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597943</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#61" center_name="The Wellcome Trust Sanger Institute" accession="ERX941435">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941435</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#61</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#61</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597946, constructed from sample accession ERS700388 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGAACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700388" refname="RNA_140619_F1-sc-1996933" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700388</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F1-sc-1996933</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597946</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#62" center_name="The Wellcome Trust Sanger Institute" accession="ERX941436">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941436</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#62</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#62</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597947, constructed from sample accession ERS700389 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700389" refname="RNA_140619_F2-sc-1996934" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700389</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F2-sc-1996934</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597947</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#63" center_name="The Wellcome Trust Sanger Institute" accession="ERX941437">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941437</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#63</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#63</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597948, constructed from sample accession ERS700390 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAAACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700390" refname="RNA_140619_F3-sc-1996935" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700390</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F3-sc-1996935</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597948</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#64" center_name="The Wellcome Trust Sanger Institute" accession="ERX941438">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941438</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#64</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#64</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597949, constructed from sample accession ERS700391 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700391" refname="RNA_140619_F4-sc-1996936" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700391</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F4-sc-1996936</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597949</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#65" center_name="The Wellcome Trust Sanger Institute" accession="ERX941439">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941439</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#65</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#65</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597950, constructed from sample accession ERS700392 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700392" refname="RNA_140619_F5-sc-1996937" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700392</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F5-sc-1996937</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597950</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#67" center_name="The Wellcome Trust Sanger Institute" accession="ERX941440">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941440</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#67</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#67</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597952, constructed from sample accession ERS700393 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700393" refname="RNA_140619_F7-sc-1996939" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700393</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F7-sc-1996939</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597952</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#68" center_name="The Wellcome Trust Sanger Institute" accession="ERX941441">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941441</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#68</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#68</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597953, constructed from sample accession ERS700394 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGACTGCATA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700394" refname="RNA_140619_F8-sc-1996940" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700394</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_F8-sc-1996940</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597953</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#73" center_name="The Wellcome Trust Sanger Institute" accession="ERX941442">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941442</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#73</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#73</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597956, constructed from sample accession ERS700395 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGAAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700395" refname="RNA_140619_G1-sc-1996943" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700395</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G1-sc-1996943</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597956</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#74" center_name="The Wellcome Trust Sanger Institute" accession="ERX941443">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941443</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#74</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#74</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597957, constructed from sample accession ERS700396 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700396" refname="RNA_140619_G2-sc-1996944" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700396</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G2-sc-1996944</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597957</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#75" center_name="The Wellcome Trust Sanger Institute" accession="ERX941444">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941444</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#75</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#75</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597958, constructed from sample accession ERS700397 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAAAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700397" refname="RNA_140619_G3-sc-1996945" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700397</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G3-sc-1996945</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597958</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#76" center_name="The Wellcome Trust Sanger Institute" accession="ERX941445">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941445</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#76</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#76</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597959, constructed from sample accession ERS700398 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700398" refname="RNA_140619_G4-sc-1996946" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700398</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G4-sc-1996946</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597959</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#77" center_name="The Wellcome Trust Sanger Institute" accession="ERX941446">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941446</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#77</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#77</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597960, constructed from sample accession ERS700399 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700399" refname="RNA_140619_G5-sc-1996947" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700399</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G5-sc-1996947</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597960</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#79" center_name="The Wellcome Trust Sanger Institute" accession="ERX941447">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941447</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#79</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#79</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597962, constructed from sample accession ERS700400 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700400" refname="RNA_140619_G7-sc-1996949" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700400</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G7-sc-1996949</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597962</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#80" center_name="The Wellcome Trust Sanger Institute" accession="ERX941448">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941448</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#80</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#80</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597963, constructed from sample accession ERS700401 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGAAGGAGTA.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700401" refname="RNA_140619_G8-sc-1996950" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700401</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_G8-sc-1996950</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597963</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#85" center_name="The Wellcome Trust Sanger Institute" accession="ERX941449">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941449</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#85</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#85</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597966, constructed from sample accession ERS700402 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TAAGGCGACTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700402" refname="RNA_140619_H1-sc-1996953" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700402</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H1-sc-1996953</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597966</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#86" center_name="The Wellcome Trust Sanger Institute" accession="ERX941450">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941450</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#86</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#86</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597967, constructed from sample accession ERS700403 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CGTACTAGCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700403" refname="RNA_140619_H2-sc-1996954" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700403</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H2-sc-1996954</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597967</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#87" center_name="The Wellcome Trust Sanger Institute" accession="ERX941451">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941451</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#87</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#87</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597968, constructed from sample accession ERS700404 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence AGGCAGAACTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700404" refname="RNA_140619_H3-sc-1996955" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700404</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H3-sc-1996955</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597968</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#88" center_name="The Wellcome Trust Sanger Institute" accession="ERX941452">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941452</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#88</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#88</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597969, constructed from sample accession ERS700405 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence TCCTGAGCCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700405" refname="RNA_140619_H4-sc-1996956" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700405</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H4-sc-1996956</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597969</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#89" center_name="The Wellcome Trust Sanger Institute" accession="ERX941453">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941453</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#89</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#89</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597970, constructed from sample accession ERS700406 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence GGACTCCTCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700406" refname="RNA_140619_H5-sc-1996957" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700406</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H5-sc-1996957</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597970</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#91" center_name="The Wellcome Trust Sanger Institute" accession="ERX941454">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941454</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#91</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#91</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597972, constructed from sample accession ERS700407 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CTCTCTACCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700407" refname="RNA_140619_H7-sc-1996959" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700407</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H7-sc-1996959</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597972</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="SC_EXP_13329_2#92" center_name="The Wellcome Trust Sanger Institute" accession="ERX941455">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX941455</PRIMARY_ID>
      <SUBMITTER_ID namespace="SC">SC_EXP_13329_2#92</SUBMITTER_ID>
      <SUBMITTER_ID namespace="The Wellcome Trust Sanger Institute">SC_EXP_13329_2#92</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2500 paired end sequencing</TITLE>
    <STUDY_REF accession="ERP010108" refname="Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603" refcenter="SC">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP010108</PRIMARY_ID>
        <SUBMITTER_ID namespace="SC">Parallel_sequencing_of_single_cell_genomes_and_transcriptomes_from_mouse_8_cell_stage_embryos-sc-3603</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Illumina sequencing of library 10597973, constructed from sample accession ERS700408 for study accession ERP010108.  This is part of an Illumina multiplexed sequencing run (13329_2).  This submission includes reads tagged with the sequence CAGAGAGGCTAAGCCT.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="ERS700408" refname="RNA_140619_H8-sc-1996960" refcenter="SC">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS700408</PRIMARY_ID>
          <SUBMITTER_ID namespace="SC">RNA_140619_H8-sc-1996960</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>10597973</LIBRARY_NAME>
        <LIBRARY_STRATEGY>RNA-Seq</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>TRANSCRIPTOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>cDNA</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="450"/>
        </LIBRARY_LAYOUT>
        <LIBRARY_CONSTRUCTION_PROTOCOL>Custom</LIBRARY_CONSTRUCTION_PROTOCOL>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
