Association tests and software for copy number variant data

<p>Abstract</p> <p>Recent studies have suggested that copy number variation (CNV) significantly contributes to genetic predisposition to several common disorders. These findings, combined with the imperfect tagging of CNVs by single nucleotide polymorphisms (SNPs), have motivated t...

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Bibliographic Details
Main Author: Plagnol Vincent
Format: Article
Language:English
Published: BMC 2009-01-01
Series:Human Genomics
Subjects:
Online Access:http://www.humgenomics.com/content/3/2/191