<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT alias="YH-fosmid_pool_12298_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894967">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894967</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12298_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12298_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12298_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12298_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12299_insertsize_316" center_name="Beijing Genome Institute" accession="ERX894968">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894968</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12299_insertsize_316</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12299_insertsize_316</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12299_insertsize_316</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12299_insertsize_316_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="316"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12299_insertsize_683" center_name="Beijing Genome Institute" accession="ERX894969">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894969</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12299_insertsize_683</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12299_insertsize_683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12299_insertsize_683</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12299_insertsize_683_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="683"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12300_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894970">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894970</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12300_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12300_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12300_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12300_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12300_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894971">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894971</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12300_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12300_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12300_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12300_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12301_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894972">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894972</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12301_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12301_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12301_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12301_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12301_insertsize_682" center_name="Beijing Genome Institute" accession="ERX894973">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894973</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12301_insertsize_682</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12301_insertsize_682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12301_insertsize_682</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12301_insertsize_682_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="682"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12302_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894974">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894974</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12302_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12302_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12302_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12302_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12302_insertsize_683" center_name="Beijing Genome Institute" accession="ERX894975">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894975</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12302_insertsize_683</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12302_insertsize_683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12302_insertsize_683</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12302_insertsize_683_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="683"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12303_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894976">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894976</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12303_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12303_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12303_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12303_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12303_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894977">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894977</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12303_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12303_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12303_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12303_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12304_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894978">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894978</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12304_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12304_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12304_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12304_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12304_insertsize_682" center_name="Beijing Genome Institute" accession="ERX894979">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894979</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12304_insertsize_682</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12304_insertsize_682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12304_insertsize_682</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12304_insertsize_682_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="682"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12305_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894980">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894980</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12305_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12305_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12305_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12305_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12305_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894981">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894981</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12305_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12305_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12305_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12305_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12306_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894982">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894982</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12306_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12306_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12306_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12306_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12306_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894983">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894983</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12306_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12306_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12306_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12306_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12307_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894984">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894984</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12307_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12307_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12307_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12307_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12307_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894985">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894985</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12307_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12307_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12307_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12307_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12308_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894986">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894986</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12308_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12308_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12308_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12308_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12308_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894987">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894987</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12308_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12308_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12308_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12308_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12309_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894988">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894988</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12309_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12309_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12309_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12309_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12309_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894989">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894989</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12309_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12309_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12309_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12309_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12315_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895001">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895001</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12315_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12315_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12315_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12315_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12316_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895002">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895002</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12316_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12316_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12316_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12316_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12316_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895003">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895003</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12316_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12316_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12316_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12316_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12317_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895004">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895004</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12317_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12317_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12317_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12317_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12317_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895005">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895005</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12317_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12317_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12317_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12317_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12318_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895006">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895006</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12318_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12318_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12318_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12318_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12318_insertsize_651" center_name="Beijing Genome Institute" accession="ERX895007">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895007</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12318_insertsize_651</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12318_insertsize_651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12318_insertsize_651</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12318_insertsize_651_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="651"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12319_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895008">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895008</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12319_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12319_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12319_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12319_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12319_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895009">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895009</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12319_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12319_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12319_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12319_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12320_insertsize_303" center_name="Beijing Genome Institute" accession="ERX895010">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895010</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12320_insertsize_303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12320_insertsize_303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12320_insertsize_303</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12320_insertsize_303_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12320_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895011">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895011</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12320_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12320_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12320_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12320_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12326_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895023">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895023</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12326_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12326_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12326_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12326_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12327_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895024">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895024</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12327_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12327_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12327_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12327_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12327_insertsize_649" center_name="Beijing Genome Institute" accession="ERX895025">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895025</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12327_insertsize_649</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12327_insertsize_649</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12327_insertsize_649</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12327_insertsize_649_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="649"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12328_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895026">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895026</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12328_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12328_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12328_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12328_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12328_insertsize_656" center_name="Beijing Genome Institute" accession="ERX895027">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895027</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12328_insertsize_656</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12328_insertsize_656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12328_insertsize_656</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12328_insertsize_656_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="656"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12329_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895028">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895028</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12329_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12329_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12329_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12329_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12329_insertsize_658" center_name="Beijing Genome Institute" accession="ERX895029">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895029</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12329_insertsize_658</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12329_insertsize_658</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12329_insertsize_658</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12329_insertsize_658_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="658"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12330_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895030">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895030</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12330_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12330_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12330_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12330_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12330_insertsize_651" center_name="Beijing Genome Institute" accession="ERX895031">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895031</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12330_insertsize_651</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12330_insertsize_651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12330_insertsize_651</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12330_insertsize_651_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="651"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12331_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895032">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895032</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12331_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12331_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12331_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12331_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12331_insertsize_657" center_name="Beijing Genome Institute" accession="ERX895033">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895033</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12331_insertsize_657</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12331_insertsize_657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12331_insertsize_657</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12331_insertsize_657_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="657"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12117_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894604">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894604</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12117_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12117_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12117_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12117_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12117_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894605">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894605</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12117_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12117_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12117_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12117_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12118_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894606">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894606</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12118_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12118_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12118_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12118_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12118_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894607">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894607</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12118_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12118_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12118_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12118_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12119_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894608">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894608</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12119_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12119_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12119_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12119_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12119_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894609">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894609</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12119_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12119_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12119_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12119_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12120_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894610">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894610</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12120_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12120_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12120_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12120_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12120_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894611">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894611</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12120_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12120_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12120_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12120_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12121_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894612">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894612</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12121_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12121_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12121_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12121_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12121_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894613">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894613</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12121_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12121_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12121_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12121_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12122_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894614">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894614</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12122_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12122_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12122_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12122_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12139_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894648">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894648</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12139_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12139_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12139_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12139_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12139_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894649">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894649</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12139_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12139_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12139_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12139_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12140_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894650">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894650</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12140_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12140_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12140_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12140_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12140_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894651">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894651</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12140_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12140_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12140_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12140_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12141_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894652">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894652</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12141_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12141_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12141_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12141_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12141_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894653">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894653</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12141_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12141_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12141_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12141_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12142_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894654">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894654</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12142_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12142_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12142_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12142_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12142_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894655">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894655</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12142_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12142_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12142_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12142_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12143_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894656">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894656</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12143_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12143_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12143_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12143_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12143_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894657">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894657</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12143_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12143_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12143_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12143_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12144_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894658">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894658</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12144_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12144_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12144_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12144_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12161_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894692">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894692</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12161_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12161_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12161_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12161_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12161_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894693">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894693</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12161_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12161_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12161_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12161_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12162_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894694">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894694</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12162_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12162_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12162_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12162_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12162_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894695">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894695</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12162_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12162_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12162_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12162_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12163_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894696">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894696</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12163_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12163_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12163_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12163_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12163_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894697">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894697</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12163_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12163_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12163_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12163_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12164_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894698">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894698</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12164_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12164_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12164_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12164_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12164_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894699">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894699</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12164_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12164_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12164_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12164_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12165_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894700">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894700</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12165_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12165_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12165_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12165_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12165_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894701">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894701</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12165_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12165_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12165_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12165_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12166_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894702">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894702</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12166_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12166_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12166_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12166_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12183_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894736">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894736</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12183_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12183_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12183_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12183_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12183_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894737">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894737</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12183_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12183_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12183_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12183_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12184_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894738">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894738</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12184_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12184_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12184_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12184_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12184_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894739">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894739</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12184_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12184_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12184_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12184_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12185_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894740">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894740</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12185_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12185_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12185_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12185_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12185_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894741">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894741</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12185_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12185_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12185_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12185_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12186_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894742">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894742</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12186_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12186_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12186_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12186_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12186_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894743">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894743</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12186_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12186_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12186_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12186_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12187_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894744">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894744</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12187_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12187_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12187_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12187_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12187_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894745">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894745</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12187_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12187_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12187_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12187_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12188_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894746">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894746</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12188_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12188_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12188_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12188_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12122_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894615">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894615</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12122_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12122_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12122_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12122_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12123_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894616">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894616</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12123_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12123_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12123_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12123_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12123_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894617">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894617</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12123_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12123_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12123_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12123_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12124_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894618">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894618</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12124_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12124_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12124_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12124_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12124_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894619">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894619</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12124_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12124_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12124_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12124_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12125_insertsize_315" center_name="Beijing Genome Institute" accession="ERX894620">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894620</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12125_insertsize_315</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12125_insertsize_315</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12125_insertsize_315</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12125_insertsize_315_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="315"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12125_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894621">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894621</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12125_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12125_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12125_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12125_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12126_insertsize_307" center_name="Beijing Genome Institute" accession="ERX894622">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894622</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12126_insertsize_307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12126_insertsize_307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12126_insertsize_307</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12126_insertsize_307_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="307"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12126_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894623">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894623</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12126_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12126_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12126_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12126_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12127_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894624">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894624</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12127_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12127_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12127_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12127_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12127_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894625">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894625</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12127_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12127_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12127_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12127_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12144_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894659">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894659</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12144_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12144_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12144_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12144_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12145_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894660">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894660</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12145_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12145_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12145_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12145_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12145_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894661">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894661</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12145_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12145_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12145_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12145_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12146_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894662">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894662</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12146_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12146_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12146_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12146_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12146_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894663">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894663</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12146_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12146_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12146_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12146_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12147_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894664">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894664</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12147_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12147_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12147_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12147_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12147_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894665">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894665</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12147_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12147_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12147_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12147_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12148_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894666">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894666</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12148_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12148_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12148_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12148_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12148_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894667">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894667</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12148_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12148_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12148_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12148_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12149_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894668">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894668</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12149_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12149_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12149_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12149_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12149_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894669">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894669</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12149_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12149_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12149_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12149_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12166_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894703">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894703</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12166_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12166_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12166_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12166_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12167_insertsize_301" center_name="Beijing Genome Institute" accession="ERX894704">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894704</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12167_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12167_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12167_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12167_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12167_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894705">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894705</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12167_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12167_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12167_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12167_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12168_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894706">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894706</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12168_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12168_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12168_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12168_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12168_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894707">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894707</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12168_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12168_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12168_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12168_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12169_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894708">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894708</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12169_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12169_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12169_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12169_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12169_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894709">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894709</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12169_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12169_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12169_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12169_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12170_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894710">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894710</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12170_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12170_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12170_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12170_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12170_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894711">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894711</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12170_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12170_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12170_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12170_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12171_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894712">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894712</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12171_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12171_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12171_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12171_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12171_insertsize_664" center_name="Beijing Genome Institute" accession="ERX894713">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894713</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12171_insertsize_664</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12171_insertsize_664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12171_insertsize_664</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12171_insertsize_664_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="664"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12188_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894747">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894747</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12188_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12188_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12188_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12188_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12189_insertsize_297" center_name="Beijing Genome Institute" accession="ERX894748">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894748</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12189_insertsize_297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12189_insertsize_297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12189_insertsize_297</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12189_insertsize_297_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="297"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12189_insertsize_672" center_name="Beijing Genome Institute" accession="ERX894749">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894749</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12189_insertsize_672</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12189_insertsize_672</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12189_insertsize_672</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12189_insertsize_672_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="672"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12190_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894750">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894750</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12190_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12190_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12190_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12190_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12190_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894751">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894751</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12190_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12190_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12190_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12190_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12191_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894752">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894752</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12191_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12191_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12191_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12191_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12191_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894753">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894753</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12191_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12191_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12191_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12191_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12192_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894754">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894754</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12192_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12192_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12192_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12192_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12192_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894755">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894755</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12192_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12192_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12192_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12192_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12193_insertsize_301" center_name="Beijing Genome Institute" accession="ERX894756">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894756</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12193_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12193_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12193_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12193_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12193_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894757">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894757</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12193_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12193_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12193_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12193_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12205_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894780">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894780</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12205_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12205_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12205_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12205_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12205_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894781">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894781</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12205_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12205_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12205_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12205_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12206_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894782">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894782</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12206_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12206_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12206_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12206_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12206_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894783">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894783</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12206_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12206_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12206_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12206_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12207_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894784">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894784</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12207_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12207_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12207_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12207_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12207_insertsize_675" center_name="Beijing Genome Institute" accession="ERX894785">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894785</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12207_insertsize_675</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12207_insertsize_675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12207_insertsize_675</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12207_insertsize_675_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="675"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12208_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894786">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894786</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12208_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12208_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12208_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12208_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12208_insertsize_675" center_name="Beijing Genome Institute" accession="ERX894787">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894787</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12208_insertsize_675</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12208_insertsize_675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12208_insertsize_675</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12208_insertsize_675_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="675"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12209_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894788">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894788</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12209_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12209_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12209_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12209_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12209_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894789">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894789</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12209_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12209_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12209_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12209_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12210_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894790">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894790</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12210_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12210_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12210_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12210_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12221_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894813">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894813</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12221_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12221_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12221_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12221_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12222_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894814">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894814</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12222_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12222_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12222_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12222_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12222_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894815">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894815</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12222_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12222_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12222_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12222_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12223_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894816">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894816</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12223_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12223_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12223_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12223_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12223_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894817">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894817</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12223_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12223_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12223_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12223_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12224_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894818">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894818</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12224_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12224_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12224_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12224_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12224_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894819">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894819</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12224_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12224_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12224_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12224_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12225_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894820">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894820</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12225_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12225_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12225_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12225_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12225_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894821">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894821</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12225_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12225_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12225_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12225_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12226_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894822">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894822</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12226_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12226_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12226_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12226_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12226_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894823">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894823</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12226_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12226_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12226_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12226_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12243_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894857">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894857</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12243_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12243_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12243_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12243_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12244_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894858">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894858</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12244_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12244_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12244_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12244_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12244_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894859">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894859</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12244_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12244_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12244_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12244_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12245_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894860">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894860</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12245_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12245_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12245_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12245_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12245_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894861">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894861</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12245_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12245_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12245_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12245_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12246_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894862">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894862</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12246_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12246_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12246_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12246_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12246_insertsize_663" center_name="Beijing Genome Institute" accession="ERX894863">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894863</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12246_insertsize_663</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12246_insertsize_663</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12246_insertsize_663</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12246_insertsize_663_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="663"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12247_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894864">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894864</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12247_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12247_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12247_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12247_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12247_insertsize_664" center_name="Beijing Genome Institute" accession="ERX894865">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894865</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12247_insertsize_664</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12247_insertsize_664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12247_insertsize_664</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12247_insertsize_664_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="664"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12248_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894866">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894866</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12248_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12248_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12248_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12248_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12248_insertsize_664" center_name="Beijing Genome Institute" accession="ERX894867">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894867</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12248_insertsize_664</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12248_insertsize_664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12248_insertsize_664</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12248_insertsize_664_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="664"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12348_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895067">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895067</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12348_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12348_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12348_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12348_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12349_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895068">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895068</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12349_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12349_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12349_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12349_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12349_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895069">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895069</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12349_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12349_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12349_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12349_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12350_insertsize_298" center_name="Beijing Genome Institute" accession="ERX895070">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895070</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12350_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12350_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12350_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12350_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12350_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895071">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895071</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12350_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12350_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12350_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12350_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12351_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895072">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895072</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12351_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12351_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12351_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12351_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12351_insertsize_660" center_name="Beijing Genome Institute" accession="ERX895073">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895073</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12351_insertsize_660</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12351_insertsize_660</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12351_insertsize_660</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12351_insertsize_660_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="660"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12352_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895074">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895074</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12352_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12352_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12352_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12352_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12352_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895075">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895075</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12352_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12352_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12352_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12352_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12353_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895076">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895076</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12353_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12353_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12353_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12353_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12353_insertsize_656" center_name="Beijing Genome Institute" accession="ERX895077">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895077</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12353_insertsize_656</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12353_insertsize_656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12353_insertsize_656</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12353_insertsize_656_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="656"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12365_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895100">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895100</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12365_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12365_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12365_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12365_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12365_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895101">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895101</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12365_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12365_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12365_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12365_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12366_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895102">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895102</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12366_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12366_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12366_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12366_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12366_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895103">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895103</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12366_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12366_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12366_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12366_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12128_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894626">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894626</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12128_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12128_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12128_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12128_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12128_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894627">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894627</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12128_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12128_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12128_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12128_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12129_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894628">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894628</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12129_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12129_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12129_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12129_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12129_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894629">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894629</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12129_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12129_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12129_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12129_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12130_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894630">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894630</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12130_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12130_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12130_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12130_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12130_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894631">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894631</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12130_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12130_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12130_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12130_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12131_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894632">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894632</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12131_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12131_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12131_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12131_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12131_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894633">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894633</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12131_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12131_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12131_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12131_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12132_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894634">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894634</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12132_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12132_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12132_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12132_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12132_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894635">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894635</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12132_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12132_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12132_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12132_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12133_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894636">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894636</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12133_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12133_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12133_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12133_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12150_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894670">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894670</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12150_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12150_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12150_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12150_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12150_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894671">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894671</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12150_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12150_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12150_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12150_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12151_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894672">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894672</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12151_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12151_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12151_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12151_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12151_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894673">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894673</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12151_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12151_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12151_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12151_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12152_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894674">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894674</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12152_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12152_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12152_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12152_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12152_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894675">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894675</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12152_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12152_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12152_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12152_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12153_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894676">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894676</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12153_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12153_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12153_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12153_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12153_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894677">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894677</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12153_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12153_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12153_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12153_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12154_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894678">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894678</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12154_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12154_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12154_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12154_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12154_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894679">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894679</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12154_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12154_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12154_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12154_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12155_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894680">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894680</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12155_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12155_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12155_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12155_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12172_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894714">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894714</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12172_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12172_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12172_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12172_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12172_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894715">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894715</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12172_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12172_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12172_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12172_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12173_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894716">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894716</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12173_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12173_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12173_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12173_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12173_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894717">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894717</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12173_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12173_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12173_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12173_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12174_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894718">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894718</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12174_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12174_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12174_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12174_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12174_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894719">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894719</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12174_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12174_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12174_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12174_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12175_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894720">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894720</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12175_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12175_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12175_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12175_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12175_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894721">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894721</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12175_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12175_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12175_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12175_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12176_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894722">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894722</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12176_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12176_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12176_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12176_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12176_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894723">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894723</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12176_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12176_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12176_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12176_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12177_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894724">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894724</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12177_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12177_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12177_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12177_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12194_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894758">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894758</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12194_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12194_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12194_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12194_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12194_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894759">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894759</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12194_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12194_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12194_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12194_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12195_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894760">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894760</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12195_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12195_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12195_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12195_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12195_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894761">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894761</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12195_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12195_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12195_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12195_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12196_insertsize_306" center_name="Beijing Genome Institute" accession="ERX894762">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894762</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12196_insertsize_306</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12196_insertsize_306</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12196_insertsize_306</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12196_insertsize_306_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="306"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12196_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894763">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894763</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12196_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12196_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12196_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12196_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12197_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894764">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894764</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12197_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12197_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12197_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12197_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12197_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894765">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894765</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12197_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12197_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12197_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12197_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12198_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894766">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894766</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12198_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12198_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12198_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12198_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12198_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894767">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894767</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12198_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12198_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12198_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12198_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12199_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894768">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894768</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12199_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12199_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12199_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12199_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12210_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894791">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894791</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12210_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12210_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12210_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12210_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12211_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894792">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894792</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12211_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12211_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12211_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12211_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12211_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894793">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894793</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12211_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12211_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12211_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12211_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12212_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894794">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894794</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12212_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12212_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12212_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12212_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12212_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894795">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894795</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12212_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12212_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12212_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12212_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12213_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894796">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894796</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12213_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12213_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12213_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12213_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12213_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894797">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894797</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12213_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12213_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12213_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12213_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12214_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894798">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894798</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12214_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12214_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12214_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12214_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12214_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894799">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894799</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12214_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12214_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12214_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12214_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12215_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894800">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894800</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12215_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12215_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12215_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12215_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12215_insertsize_675" center_name="Beijing Genome Institute" accession="ERX894801">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894801</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12215_insertsize_675</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12215_insertsize_675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12215_insertsize_675</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12215_insertsize_675_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="675"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12227_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894824">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894824</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12227_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12227_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12227_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12227_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12227_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894825">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894825</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12227_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12227_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12227_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12227_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12228_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894826">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894826</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12228_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12228_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12228_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12228_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12228_insertsize_675" center_name="Beijing Genome Institute" accession="ERX894827">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894827</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12228_insertsize_675</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12228_insertsize_675</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12228_insertsize_675</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12228_insertsize_675_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="675"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12229_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894828">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894828</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12229_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12229_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12229_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12229_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12229_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894829">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894829</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12229_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12229_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12229_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12229_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12230_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894830">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894830</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12230_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12230_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12230_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12230_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12230_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894831">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894831</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12230_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12230_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12230_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12230_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12231_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894832">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894832</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12231_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12231_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12231_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12231_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12231_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894833">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894833</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12231_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12231_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12231_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12231_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12232_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894834">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894834</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12232_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12232_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12232_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12232_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12249_insertsize_319" center_name="Beijing Genome Institute" accession="ERX894868">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894868</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12249_insertsize_319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12249_insertsize_319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12249_insertsize_319</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12249_insertsize_319_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12249_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894869">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894869</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12249_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12249_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12249_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12249_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12250_insertsize_319" center_name="Beijing Genome Institute" accession="ERX894870">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894870</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12250_insertsize_319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12250_insertsize_319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12250_insertsize_319</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12250_insertsize_319_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12250_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894871">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894871</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12250_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12250_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12250_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12250_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12251_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894872">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894872</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12251_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12251_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12251_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12251_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12251_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894873">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894873</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12251_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12251_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12251_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12251_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12252_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894874">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894874</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12252_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12252_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12252_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12252_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12252_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894875">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894875</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12252_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12252_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12252_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12252_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12253_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894876">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894876</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12253_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12253_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12253_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12253_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12253_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894877">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894877</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12253_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12253_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12253_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12253_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12254_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894878">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894878</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12254_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12254_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12254_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12254_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12265_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894901">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894901</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12265_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12265_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12265_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12265_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12266_insertsize_319" center_name="Beijing Genome Institute" accession="ERX894902">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894902</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12266_insertsize_319</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12266_insertsize_319</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12266_insertsize_319</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12266_insertsize_319_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="319"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12266_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894903">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894903</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12266_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12266_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12266_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12266_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12267_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894904">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894904</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12267_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12267_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12267_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12267_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12267_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894905">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894905</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12267_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12267_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12267_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12267_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12268_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894906">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894906</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12268_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12268_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12268_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12268_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12268_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894907">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894907</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12268_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12268_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12268_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12268_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12269_insertsize_323" center_name="Beijing Genome Institute" accession="ERX894908">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894908</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12269_insertsize_323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12269_insertsize_323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12269_insertsize_323</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12269_insertsize_323_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="323"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12269_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894909">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894909</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12269_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12269_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12269_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12269_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12270_insertsize_323" center_name="Beijing Genome Institute" accession="ERX894910">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894910</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12270_insertsize_323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12270_insertsize_323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12270_insertsize_323</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12270_insertsize_323_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="323"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12270_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894911">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894911</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12270_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12270_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12270_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12270_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12133_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894637">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894637</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12133_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12133_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12133_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12133_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12134_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894638">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894638</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12134_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12134_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12134_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12134_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12134_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894639">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894639</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12134_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12134_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12134_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12134_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12135_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894640">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894640</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12135_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12135_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12135_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12135_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12135_insertsize_672" center_name="Beijing Genome Institute" accession="ERX894641">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894641</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12135_insertsize_672</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12135_insertsize_672</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12135_insertsize_672</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12135_insertsize_672_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="672"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12136_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894642">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894642</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12136_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12136_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12136_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12136_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12136_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894643">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894643</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12136_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12136_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12136_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12136_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12137_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894644">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894644</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12137_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12137_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12137_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12137_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12137_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894645">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894645</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12137_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12137_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12137_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12137_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12138_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894646">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894646</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12138_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12138_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12138_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12138_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12138_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894647">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894647</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12138_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12138_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12138_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12138_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12155_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894681">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894681</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12155_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12155_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12155_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12155_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12156_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894682">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894682</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12156_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12156_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12156_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12156_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12156_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894683">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894683</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12156_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12156_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12156_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12156_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12157_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894684">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894684</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12157_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12157_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12157_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12157_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12157_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894685">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894685</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12157_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12157_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12157_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12157_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12158_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894686">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894686</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12158_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12158_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12158_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12158_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12158_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894687">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894687</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12158_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12158_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12158_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12158_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12159_insertsize_301" center_name="Beijing Genome Institute" accession="ERX894688">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894688</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12159_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12159_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12159_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12159_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12159_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894689">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894689</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12159_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12159_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12159_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12159_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12160_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894690">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894690</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12160_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12160_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12160_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12160_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12160_insertsize_671" center_name="Beijing Genome Institute" accession="ERX894691">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894691</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12160_insertsize_671</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12160_insertsize_671</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12160_insertsize_671</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12160_insertsize_671_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="671"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12177_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894725">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894725</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12177_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12177_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12177_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12177_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12178_insertsize_299" center_name="Beijing Genome Institute" accession="ERX894726">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894726</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12178_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12178_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12178_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12178_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12178_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894727">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894727</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12178_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12178_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12178_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12178_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12179_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894728">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894728</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12179_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12179_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12179_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12179_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12179_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894729">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894729</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12179_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12179_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12179_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12179_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12180_insertsize_300" center_name="Beijing Genome Institute" accession="ERX894730">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894730</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12180_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12180_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12180_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12180_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12180_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894731">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894731</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12180_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12180_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12180_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12180_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12181_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894732">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894732</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12181_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12181_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12181_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12181_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12181_insertsize_670" center_name="Beijing Genome Institute" accession="ERX894733">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894733</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12181_insertsize_670</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12181_insertsize_670</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12181_insertsize_670</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12181_insertsize_670_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="670"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12182_insertsize_298" center_name="Beijing Genome Institute" accession="ERX894734">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894734</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12182_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12182_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12182_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12182_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12182_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894735">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894735</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12182_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12182_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12182_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12182_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12199_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894769">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894769</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12199_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12199_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12199_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12199_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12200_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894770">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894770</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12200_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12200_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12200_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12200_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12200_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894771">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894771</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12200_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12200_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12200_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12200_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12201_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894772">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894772</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12201_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12201_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12201_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12201_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12201_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894773">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894773</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12201_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12201_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12201_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12201_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12202_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894774">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894774</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12202_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12202_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12202_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12202_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12202_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894775">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894775</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12202_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12202_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12202_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12202_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12203_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894776">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894776</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12203_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12203_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12203_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12203_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12203_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894777">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894777</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12203_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12203_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12203_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12203_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12204_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894778">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894778</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12204_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12204_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12204_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12204_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12204_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894779">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894779</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12204_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12204_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12204_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12204_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12216_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894802">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894802</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12216_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12216_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12216_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12216_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12216_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894803">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894803</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12216_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12216_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12216_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12216_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12217_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894804">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894804</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12217_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12217_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12217_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12217_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12217_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894805">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894805</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12217_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12217_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12217_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12217_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12218_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894806">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894806</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12218_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12218_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12218_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12218_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12218_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894807">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894807</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12218_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12218_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12218_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12218_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12219_insertsize_307" center_name="Beijing Genome Institute" accession="ERX894808">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894808</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12219_insertsize_307</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12219_insertsize_307</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12219_insertsize_307</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12219_insertsize_307_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="307"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12219_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894809">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894809</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12219_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12219_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12219_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12219_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12220_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894810">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894810</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12220_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12220_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12220_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12220_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12220_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894811">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894811</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12220_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12220_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12220_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12220_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12221_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894812">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894812</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12221_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12221_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12221_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12221_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12232_insertsize_676" center_name="Beijing Genome Institute" accession="ERX894835">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894835</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12232_insertsize_676</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12232_insertsize_676</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12232_insertsize_676</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12232_insertsize_676_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="676"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12233_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894836">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894836</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12233_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12233_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12233_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12233_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12233_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894837">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894837</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12233_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12233_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12233_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12233_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12234_insertsize_308" center_name="Beijing Genome Institute" accession="ERX894838">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894838</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12234_insertsize_308</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12234_insertsize_308</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12234_insertsize_308</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12234_insertsize_308_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="308"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12234_insertsize_674" center_name="Beijing Genome Institute" accession="ERX894839">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894839</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12234_insertsize_674</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12234_insertsize_674</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12234_insertsize_674</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12234_insertsize_674_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="674"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12235_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894840">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894840</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12235_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12235_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12235_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12235_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12235_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894841">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894841</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12235_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12235_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12235_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12235_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12236_insertsize_324" center_name="Beijing Genome Institute" accession="ERX894842">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894842</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12236_insertsize_324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12236_insertsize_324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12236_insertsize_324</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12236_insertsize_324_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12236_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894843">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894843</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12236_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12236_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12236_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12236_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12237_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894844">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894844</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12237_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12237_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12237_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12237_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12237_insertsize_664" center_name="Beijing Genome Institute" accession="ERX894845">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894845</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12237_insertsize_664</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12237_insertsize_664</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12237_insertsize_664</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12237_insertsize_664_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="664"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12254_insertsize_673" center_name="Beijing Genome Institute" accession="ERX894879">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894879</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12254_insertsize_673</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12254_insertsize_673</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12254_insertsize_673</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12254_insertsize_673_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="673"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12255_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894880">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894880</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12255_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12255_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12255_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12255_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12255_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894881">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894881</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12255_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12255_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12255_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12255_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12256_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894882">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894882</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12256_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12256_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12256_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12256_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12256_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894883">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894883</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12256_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12256_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12256_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12256_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12257_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894884">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894884</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12257_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12257_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12257_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12257_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12257_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894885">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894885</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12257_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12257_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12257_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12257_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12258_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894886">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894886</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12258_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12258_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12258_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12258_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12258_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894887">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894887</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12258_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12258_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12258_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12258_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12259_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894888">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894888</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12259_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12259_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12259_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12259_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12259_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894889">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894889</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12259_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12259_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12259_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12259_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12271_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894912">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894912</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12271_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12271_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12271_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12271_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12271_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894913">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894913</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12271_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12271_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12271_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12271_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12272_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894914">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894914</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12272_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12272_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12272_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12272_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12272_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894915">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894915</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12272_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12272_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12272_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12272_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12273_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894916">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894916</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12273_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12273_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12273_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12273_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12273_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894917">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894917</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12273_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12273_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12273_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12273_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12274_insertsize_323" center_name="Beijing Genome Institute" accession="ERX894918">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894918</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12274_insertsize_323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12274_insertsize_323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12274_insertsize_323</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12274_insertsize_323_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="323"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12274_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894919">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894919</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12274_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12274_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12274_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12274_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12275_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894920">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894920</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12275_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12275_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12275_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12275_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12275_insertsize_685" center_name="Beijing Genome Institute" accession="ERX894921">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894921</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12275_insertsize_685</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12275_insertsize_685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12275_insertsize_685</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12275_insertsize_685_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="685"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12276_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894922">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894922</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12276_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12276_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12276_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12276_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12282_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894934">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894934</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12282_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12282_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12282_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12282_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12282_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894935">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894935</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12282_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12282_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12282_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12282_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12283_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894936">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894936</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12283_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12283_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12283_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12283_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12283_insertsize_684" center_name="Beijing Genome Institute" accession="ERX894937">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894937</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12283_insertsize_684</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12283_insertsize_684</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12283_insertsize_684</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12283_insertsize_684_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="684"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12284_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894938">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894938</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12284_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12284_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12284_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12284_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12284_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894939">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894939</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12284_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12284_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12284_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12284_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12285_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894940">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894940</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12285_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12285_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12285_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12285_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12285_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894941">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894941</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12285_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12285_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12285_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12285_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12286_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894942">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894942</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12286_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12286_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12286_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12286_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12286_insertsize_685" center_name="Beijing Genome Institute" accession="ERX894943">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894943</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12286_insertsize_685</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12286_insertsize_685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12286_insertsize_685</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12286_insertsize_685_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="685"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12287_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894944">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894944</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12287_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12287_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12287_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12287_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12238_insertsize_324" center_name="Beijing Genome Institute" accession="ERX894846">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894846</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12238_insertsize_324</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12238_insertsize_324</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12238_insertsize_324</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12238_insertsize_324_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="324"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12238_insertsize_669" center_name="Beijing Genome Institute" accession="ERX894847">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894847</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12238_insertsize_669</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12238_insertsize_669</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12238_insertsize_669</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12238_insertsize_669_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="669"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12239_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894848">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894848</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12239_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12239_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12239_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12239_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12239_insertsize_665" center_name="Beijing Genome Institute" accession="ERX894849">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894849</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12239_insertsize_665</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12239_insertsize_665</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12239_insertsize_665</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12239_insertsize_665_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="665"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12240_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894850">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894850</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12240_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12240_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12240_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12240_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12240_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894851">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894851</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12240_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12240_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12240_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12240_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12241_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894852">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894852</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12241_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12241_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12241_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12241_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12241_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894853">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894853</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12241_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12241_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12241_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12241_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12242_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894854">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894854</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12242_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12242_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12242_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12242_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12242_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894855">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894855</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12242_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12242_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12242_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12242_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12243_insertsize_320" center_name="Beijing Genome Institute" accession="ERX894856">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894856</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12243_insertsize_320</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12243_insertsize_320</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12243_insertsize_320</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12243_insertsize_320_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="320"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12260_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894890">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894890</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12260_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12260_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12260_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12260_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12260_insertsize_666" center_name="Beijing Genome Institute" accession="ERX894891">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894891</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12260_insertsize_666</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12260_insertsize_666</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12260_insertsize_666</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12260_insertsize_666_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="666"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12261_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894892">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894892</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12261_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12261_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12261_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12261_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12261_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894893">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894893</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12261_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12261_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12261_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12261_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12262_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894894">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894894</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12262_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12262_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12262_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12262_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12262_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894895">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894895</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12262_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12262_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12262_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12262_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12263_insertsize_321" center_name="Beijing Genome Institute" accession="ERX894896">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894896</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12263_insertsize_321</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12263_insertsize_321</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12263_insertsize_321</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12263_insertsize_321_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="321"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12263_insertsize_667" center_name="Beijing Genome Institute" accession="ERX894897">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894897</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12263_insertsize_667</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12263_insertsize_667</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12263_insertsize_667</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12263_insertsize_667_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="667"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12264_insertsize_322" center_name="Beijing Genome Institute" accession="ERX894898">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894898</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12264_insertsize_322</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12264_insertsize_322</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12264_insertsize_322</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12264_insertsize_322_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="322"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12264_insertsize_668" center_name="Beijing Genome Institute" accession="ERX894899">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894899</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12264_insertsize_668</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12264_insertsize_668</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12264_insertsize_668</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12264_insertsize_668_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="668"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12265_insertsize_323" center_name="Beijing Genome Institute" accession="ERX894900">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894900</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12265_insertsize_323</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12265_insertsize_323</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12265_insertsize_323</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12265_insertsize_323_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="323"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12276_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894923">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894923</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12276_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12276_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12276_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12276_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12277_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894924">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894924</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12277_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12277_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12277_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12277_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12277_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894925">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894925</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12277_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12277_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12277_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12277_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12278_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894926">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894926</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12278_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12278_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12278_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12278_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12278_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894927">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894927</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12278_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12278_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12278_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12278_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12279_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894928">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894928</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12279_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12279_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12279_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12279_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12279_insertsize_683" center_name="Beijing Genome Institute" accession="ERX894929">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894929</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12279_insertsize_683</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12279_insertsize_683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12279_insertsize_683</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12279_insertsize_683_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="683"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12280_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894930">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894930</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12280_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12280_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12280_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12280_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12280_insertsize_677" center_name="Beijing Genome Institute" accession="ERX894931">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894931</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12280_insertsize_677</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12280_insertsize_677</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12280_insertsize_677</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12280_insertsize_677_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="677"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12281_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894932">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894932</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12281_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12281_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12281_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12281_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12281_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894933">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894933</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12281_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12281_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12281_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12281_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12287_insertsize_678" center_name="Beijing Genome Institute" accession="ERX894945">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894945</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12287_insertsize_678</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12287_insertsize_678</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12287_insertsize_678</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12287_insertsize_678_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="678"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12288_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894946">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894946</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12288_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12288_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12288_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12288_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12288_insertsize_684" center_name="Beijing Genome Institute" accession="ERX894947">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894947</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12288_insertsize_684</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12288_insertsize_684</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12288_insertsize_684</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12288_insertsize_684_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="684"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12289_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894948">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894948</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12289_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12289_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12289_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12289_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12289_insertsize_685" center_name="Beijing Genome Institute" accession="ERX894949">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894949</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12289_insertsize_685</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12289_insertsize_685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12289_insertsize_685</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12289_insertsize_685_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="685"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12290_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894950">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894950</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12290_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12290_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12290_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12290_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12290_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894951">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894951</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12290_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12290_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12290_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12290_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12291_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894952">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894952</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12291_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12291_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12291_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12291_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12291_insertsize_683" center_name="Beijing Genome Institute" accession="ERX894953">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894953</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12291_insertsize_683</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12291_insertsize_683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12291_insertsize_683</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12291_insertsize_683_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="683"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12292_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894954">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894954</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12292_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12292_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12292_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12292_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12292_insertsize_682" center_name="Beijing Genome Institute" accession="ERX894955">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894955</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12292_insertsize_682</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12292_insertsize_682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12292_insertsize_682</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12292_insertsize_682_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="682"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12293_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894956">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894956</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12293_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12293_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12293_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12293_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12293_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894957">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894957</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12293_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12293_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12293_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12293_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12294_insertsize_309" center_name="Beijing Genome Institute" accession="ERX894958">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894958</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12294_insertsize_309</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12294_insertsize_309</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12294_insertsize_309</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12294_insertsize_309_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="309"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12294_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894959">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894959</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12294_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12294_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12294_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12294_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12295_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894960">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894960</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12295_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12295_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12295_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12295_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12295_insertsize_683" center_name="Beijing Genome Institute" accession="ERX894961">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894961</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12295_insertsize_683</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12295_insertsize_683</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12295_insertsize_683</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12295_insertsize_683_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="683"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12296_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894962">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894962</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12296_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12296_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12296_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12296_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12296_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894963">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894963</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12296_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12296_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12296_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12296_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12297_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894964">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894964</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12297_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12297_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12297_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12297_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12297_insertsize_679" center_name="Beijing Genome Institute" accession="ERX894965">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894965</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12297_insertsize_679</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12297_insertsize_679</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12297_insertsize_679</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12297_insertsize_679_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="679"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12298_insertsize_310" center_name="Beijing Genome Institute" accession="ERX894966">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894966</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12298_insertsize_310</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12298_insertsize_310</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12298_insertsize_310</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12298_insertsize_310_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="310"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12337_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895045">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895045</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12337_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12337_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12337_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12337_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12338_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895046">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895046</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12338_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12338_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12338_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12338_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12338_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895047">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895047</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12338_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12338_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12338_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12338_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12339_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895048">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895048</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12339_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12339_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12339_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12339_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12339_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895049">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895049</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12339_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12339_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12339_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12339_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12340_insertsize_297" center_name="Beijing Genome Institute" accession="ERX895050">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895050</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12340_insertsize_297</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12340_insertsize_297</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12340_insertsize_297</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12340_insertsize_297_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="297"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12340_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895051">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895051</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12340_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12340_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12340_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12340_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12341_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895052">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895052</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12341_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12341_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12341_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12341_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12341_insertsize_651" center_name="Beijing Genome Institute" accession="ERX895053">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895053</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12341_insertsize_651</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12341_insertsize_651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12341_insertsize_651</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12341_insertsize_651_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="651"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12342_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895054">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895054</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12342_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12342_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12342_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12342_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12342_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895055">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895055</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12342_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12342_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12342_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12342_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12354_insertsize_298" center_name="Beijing Genome Institute" accession="ERX895078">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895078</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12354_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12354_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12354_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12354_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12354_insertsize_651" center_name="Beijing Genome Institute" accession="ERX895079">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895079</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12354_insertsize_651</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12354_insertsize_651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12354_insertsize_651</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12354_insertsize_651_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="651"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12355_insertsize_303" center_name="Beijing Genome Institute" accession="ERX895080">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895080</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12355_insertsize_303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12355_insertsize_303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12355_insertsize_303</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12355_insertsize_303_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12355_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895081">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895081</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12355_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12355_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12355_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12355_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12356_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895082">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895082</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12356_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12356_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12356_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12356_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12356_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895083">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895083</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12356_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12356_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12356_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12356_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12357_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895084">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895084</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12357_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12357_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12357_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12357_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12357_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895085">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895085</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12357_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12357_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12357_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12357_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12358_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895086">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895086</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12358_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12358_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12358_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12358_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12358_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895087">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895087</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12358_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12358_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12358_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12358_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12359_insertsize_304" center_name="Beijing Genome Institute" accession="ERX895088">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895088</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12359_insertsize_304</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12359_insertsize_304</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12359_insertsize_304</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12359_insertsize_304_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="304"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12310_insertsize_314" center_name="Beijing Genome Institute" accession="ERX894990">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894990</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12310_insertsize_314</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12310_insertsize_314</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12310_insertsize_314</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12310_insertsize_314_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="314"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12310_insertsize_682" center_name="Beijing Genome Institute" accession="ERX894991">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894991</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12310_insertsize_682</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12310_insertsize_682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12310_insertsize_682</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12310_insertsize_682_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="682"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12311_insertsize_311" center_name="Beijing Genome Institute" accession="ERX894992">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894992</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12311_insertsize_311</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12311_insertsize_311</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12311_insertsize_311</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12311_insertsize_311_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="311"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12311_insertsize_685" center_name="Beijing Genome Institute" accession="ERX894993">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894993</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12311_insertsize_685</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12311_insertsize_685</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12311_insertsize_685</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12311_insertsize_685_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="685"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12312_insertsize_313" center_name="Beijing Genome Institute" accession="ERX894994">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894994</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12312_insertsize_313</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12312_insertsize_313</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12312_insertsize_313</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12312_insertsize_313_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="313"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12312_insertsize_681" center_name="Beijing Genome Institute" accession="ERX894995">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894995</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12312_insertsize_681</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12312_insertsize_681</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12312_insertsize_681</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12312_insertsize_681_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="681"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12313_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894996">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894996</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12313_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12313_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12313_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12313_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12313_insertsize_682" center_name="Beijing Genome Institute" accession="ERX894997">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894997</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12313_insertsize_682</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12313_insertsize_682</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12313_insertsize_682</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12313_insertsize_682_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="682"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12314_insertsize_312" center_name="Beijing Genome Institute" accession="ERX894998">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894998</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12314_insertsize_312</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12314_insertsize_312</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12314_insertsize_312</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12314_insertsize_312_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="312"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12314_insertsize_680" center_name="Beijing Genome Institute" accession="ERX894999">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX894999</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12314_insertsize_680</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12314_insertsize_680</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12314_insertsize_680</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12314_insertsize_680_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="680"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12315_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895000">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895000</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12315_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12315_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12315_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12315_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12321_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895012">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895012</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12321_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12321_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12321_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12321_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12321_insertsize_656" center_name="Beijing Genome Institute" accession="ERX895013">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895013</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12321_insertsize_656</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12321_insertsize_656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12321_insertsize_656</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12321_insertsize_656_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="656"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12322_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895014">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895014</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12322_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12322_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12322_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12322_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12322_insertsize_656" center_name="Beijing Genome Institute" accession="ERX895015">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895015</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12322_insertsize_656</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12322_insertsize_656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12322_insertsize_656</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12322_insertsize_656_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="656"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12323_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895016">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895016</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12323_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12323_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12323_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12323_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12323_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895017">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895017</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12323_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12323_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12323_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12323_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12324_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895018">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895018</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12324_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12324_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12324_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12324_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12324_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895019">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895019</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12324_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12324_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12324_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12324_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12325_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895020">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895020</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12325_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12325_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12325_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12325_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12325_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895021">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895021</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12325_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12325_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12325_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12325_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12326_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895022">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895022</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12326_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12326_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12326_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12326_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12332_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895034">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895034</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12332_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12332_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12332_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12332_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12332_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895035">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895035</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12332_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12332_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12332_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12332_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12333_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895036">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895036</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12333_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12333_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12333_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12333_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12333_insertsize_656" center_name="Beijing Genome Institute" accession="ERX895037">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895037</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12333_insertsize_656</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12333_insertsize_656</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12333_insertsize_656</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12333_insertsize_656_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="656"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12334_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895038">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895038</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12334_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12334_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12334_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12334_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12334_insertsize_653" center_name="Beijing Genome Institute" accession="ERX895039">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895039</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12334_insertsize_653</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12334_insertsize_653</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12334_insertsize_653</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12334_insertsize_653_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="653"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12335_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895040">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895040</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12335_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12335_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12335_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12335_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12335_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895041">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895041</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12335_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12335_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12335_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12335_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12336_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895042">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895042</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12336_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12336_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12336_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12336_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12336_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895043">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895043</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12336_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12336_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12336_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12336_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12337_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895044">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895044</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12337_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12337_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12337_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12337_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12343_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895056">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895056</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12343_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12343_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12343_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12343_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12343_insertsize_655" center_name="Beijing Genome Institute" accession="ERX895057">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895057</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12343_insertsize_655</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12343_insertsize_655</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12343_insertsize_655</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12343_insertsize_655_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="655"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12344_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895058">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895058</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12344_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12344_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12344_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12344_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12344_insertsize_650" center_name="Beijing Genome Institute" accession="ERX895059">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895059</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12344_insertsize_650</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12344_insertsize_650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12344_insertsize_650</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12344_insertsize_650_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="650"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12345_insertsize_301" center_name="Beijing Genome Institute" accession="ERX895060">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895060</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12345_insertsize_301</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12345_insertsize_301</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12345_insertsize_301</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12345_insertsize_301_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="301"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12345_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895061">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895061</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12345_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12345_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12345_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12345_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12346_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895062">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895062</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12346_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12346_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12346_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12346_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12346_insertsize_657" center_name="Beijing Genome Institute" accession="ERX895063">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895063</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12346_insertsize_657</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12346_insertsize_657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12346_insertsize_657</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12346_insertsize_657_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="657"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12347_insertsize_298" center_name="Beijing Genome Institute" accession="ERX895064">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895064</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12347_insertsize_298</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12347_insertsize_298</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12347_insertsize_298</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12347_insertsize_298_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="298"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12347_insertsize_657" center_name="Beijing Genome Institute" accession="ERX895065">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895065</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12347_insertsize_657</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12347_insertsize_657</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12347_insertsize_657</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12347_insertsize_657_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="657"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12348_insertsize_299" center_name="Beijing Genome Institute" accession="ERX895066">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895066</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12348_insertsize_299</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12348_insertsize_299</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12348_insertsize_299</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12348_insertsize_299_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="299"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12360_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895090">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895090</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12360_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12360_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12360_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12360_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12360_insertsize_654" center_name="Beijing Genome Institute" accession="ERX895091">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895091</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12360_insertsize_654</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12360_insertsize_654</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12360_insertsize_654</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12360_insertsize_654_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="654"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12361_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895092">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895092</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12361_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12361_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12361_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12361_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12361_insertsize_650" center_name="Beijing Genome Institute" accession="ERX895093">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895093</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12361_insertsize_650</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12361_insertsize_650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12361_insertsize_650</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12361_insertsize_650_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="650"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12362_insertsize_303" center_name="Beijing Genome Institute" accession="ERX895094">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895094</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12362_insertsize_303</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12362_insertsize_303</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12362_insertsize_303</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12362_insertsize_303_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="303"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12362_insertsize_649" center_name="Beijing Genome Institute" accession="ERX895095">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895095</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12362_insertsize_649</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12362_insertsize_649</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12362_insertsize_649</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12362_insertsize_649_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="649"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12363_insertsize_302" center_name="Beijing Genome Institute" accession="ERX895096">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895096</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12363_insertsize_302</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12363_insertsize_302</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12363_insertsize_302</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12363_insertsize_302_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="302"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12363_insertsize_650" center_name="Beijing Genome Institute" accession="ERX895097">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895097</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12363_insertsize_650</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12363_insertsize_650</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12363_insertsize_650</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12363_insertsize_650_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="650"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12364_insertsize_300" center_name="Beijing Genome Institute" accession="ERX895098">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895098</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12364_insertsize_300</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12364_insertsize_300</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12364_insertsize_300</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12364_insertsize_300_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="300"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12364_insertsize_652" center_name="Beijing Genome Institute" accession="ERX895099">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895099</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12364_insertsize_652</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12364_insertsize_652</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12364_insertsize_652</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12364_insertsize_652_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="652"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT alias="YH-fosmid_pool_12359_insertsize_651" center_name="Beijing Genome Institute" accession="ERX895089">
    <IDENTIFIERS>
      <PRIMARY_ID>ERX895089</PRIMARY_ID>
      <SUBMITTER_ID namespace="BGI">YH-fosmid_pool_12359_insertsize_651</SUBMITTER_ID>
      <SUBMITTER_ID namespace="Beijing Genome Institute">YH-fosmid_pool_12359_insertsize_651</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>Illumina HiSeq 2000 paired end sequencing; YH-fosmid_pool_12359_insertsize_651</TITLE>
    <STUDY_REF accession="ERP008872" refname="ena-STUDY-BGI-28-11-2014-05:54:57:413-2190" refcenter="BGI">
      <IDENTIFIERS>
        <PRIMARY_ID>ERP008872</PRIMARY_ID>
        <SUBMITTER_ID namespace="BGI">ena-STUDY-BGI-28-11-2014-05:54:57:413-2190</SUBMITTER_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>We pooled ~30 fosmid clones and sequenced using Hiseq 2000 with different insertion sizes. We estimated that, on average, each pool contained only 0.02% of the diploid genome, therefore the DNA in each pool represented small portions of different regions on the genome and the probability that any two fosmids came from the same/overlapping genomic region was near zero.</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR refname="YH_cell_line" accession="ERS631797" refcenter="BGI">
        <IDENTIFIERS>
          <PRIMARY_ID>ERS631797</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMEA3178893</EXTERNAL_ID>
          <SUBMITTER_ID namespace="BGI">YH_cell_line</SUBMITTER_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>YH-fosmid_pool_12359_insertsize_651_lib</LIBRARY_NAME>
        <LIBRARY_STRATEGY>POOLCLONE</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>RANDOM</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED NOMINAL_LENGTH="651"/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2000</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
