Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies.
Genome-wide association scans (GWASs) using single nucleotide polymorphisms (SNPs) have been completed successfully for several common disorders and have detected over 30 new associations. Considering the large sample sizes and genome-wide SNP coverage of the scans, one might have expected many of t...
Main Authors: | Xavier Estivill, Lluís Armengol |
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Format: | Article |
Language: | English |
Published: |
Public Library of Science (PLoS)
2007-10-01
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Series: | PLoS Genetics |
Online Access: | http://europepmc.org/articles/PMC2039766?pdf=render |
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