Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation

被引：0
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作者：
Laura E MacConaill
Micheala A Aldred
Xincheng Lu
Thomas LaFramboise
机构：
[1] Dana-Farber Cancer Institute,Genomic Medicine Institute, Lerner Research Institute
[2] The Broad Institute of Harvard and MIT,Department of Genetics
[3] Cleveland Clinic,undefined
[4] Case Western Reserve University,undefined
来源：
BMC Genomics | / 8卷
关键词：
Copy Number Variant; Additional Data File; Segmental Duplication; Reference Panel; Generalize Genotype;
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