<?xml version="1.0" encoding="UTF-8"?>
<EXPERIMENT_SET xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance">
  <EXPERIMENT accession="SRX2769676" alias="NA00682_v1MADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769676</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">NA00682_v1MADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>v1MADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, 8000 common SNPs, targeted region in file "v1MADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NA00682_v1MADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769677" alias="NA00503_v1MADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769677</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">NA00503_v1MADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>v1MADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, 8000 common SNPs, targeted region in file "v1MADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NA00503_v1MADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769678" alias="GM19239_v1MADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769678</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">GM19239_v1MADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>v1MADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, 8000 common SNPs, targeted region in file "v1MADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GM19239_v1MADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769679" alias="GM06990_v1MADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769679</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">GM06990_v1MADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>v1MADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, 8000 common SNPs, targeted region in file "v1MADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GM06990_v1MADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769680" alias="AG13074_v1MADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769680</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">AG13074_v1MADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>v1MADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, 8000 common SNPs, targeted region in file "v1MADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AG13074_v1MADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769681" alias="H1_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769681</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">H1_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: H1 ES cell line</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153296">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153296</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842816</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>H1_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769682" alias="NA01454_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769682</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">NA01454_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153297">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153297</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842815</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NA01454_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769683" alias="NA00682_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769683</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">NA00682_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153291">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153291</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842814</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NA00682_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769684" alias="NA00503_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769684</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">NA00503_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153292">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153292</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842813</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>NA00503_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769685" alias="HG01939_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769685</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">HG01939_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153298">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153298</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842812</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>HG01939_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769686" alias="GM19239_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769686</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">GM19239_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153293">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153293</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842811</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GM19239_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769687" alias="GM06990_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769687</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">GM06990_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: LCL</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153294">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153294</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842810</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GM06990_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769688" alias="GM00496_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769688</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">GM00496_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153299">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153299</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842809</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>GM00496_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
  <EXPERIMENT accession="SRX2769689" alias="AG13074_meMADseq">
    <IDENTIFIERS>
      <PRIMARY_ID>SRX2769689</PRIMARY_ID>
      <SUBMITTER_ID namespace="SUB2612372">AG13074_meMADseq</SUBMITTER_ID>
    </IDENTIFIERS>
    <TITLE>meMADseq of human: fibroblast</TITLE>
    <STUDY_REF accession="SRP105435">
      <IDENTIFIERS>
        <PRIMARY_ID>SRP105435</PRIMARY_ID>
        <EXTERNAL_ID namespace="BioProject">PRJNA384616</EXTERNAL_ID>
      </IDENTIFIERS>
    </STUDY_REF>
    <DESIGN>
      <DESIGN_DESCRIPTION>Roche NimbleGen SeqCap EZ Choice system, Design Identifier: 160407_HG19_MadSeq_EZ_HX1 (meMADseq), targeted region in file "meMADseq.target.hg19.bed"</DESIGN_DESCRIPTION>
      <SAMPLE_DESCRIPTOR accession="SRS2153295">
        <IDENTIFIERS>
          <PRIMARY_ID>SRS2153295</PRIMARY_ID>
          <EXTERNAL_ID namespace="BioSample">SAMN06842808</EXTERNAL_ID>
        </IDENTIFIERS>
      </SAMPLE_DESCRIPTOR>
      <LIBRARY_DESCRIPTOR>
        <LIBRARY_NAME>AG13074_meMADseq</LIBRARY_NAME>
        <LIBRARY_STRATEGY>WCS</LIBRARY_STRATEGY>
        <LIBRARY_SOURCE>GENOMIC</LIBRARY_SOURCE>
        <LIBRARY_SELECTION>Hybrid Selection</LIBRARY_SELECTION>
        <LIBRARY_LAYOUT>
          <PAIRED/>
        </LIBRARY_LAYOUT>
      </LIBRARY_DESCRIPTOR>
    </DESIGN>
    <PLATFORM>
      <ILLUMINA>
        <INSTRUMENT_MODEL>Illumina HiSeq 2500</INSTRUMENT_MODEL>
      </ILLUMINA>
    </PLATFORM>
  </EXPERIMENT>
</EXPERIMENT_SET>
