Toward accurate high-throughput SNP genotyping in the presence of inherited copy number variation
<p>Abstract</p> <p>Background</p> <p>The recent discovery of widespread copy number variation in humans has forced a shift away from the assumption of two copies per locus per cell throughout the autosomal genome. In particular, a SNP site can no longer always be accura...
Main Authors: | , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2007-07-01
|
Series: | BMC Genomics |
Online Access: | http://www.biomedcentral.com/1471-2164/8/211 |