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