Llwytho...

A robust statistical method for case-control association testing with copy number variation

Copy number variation (CNV) is pervasive in the human genome and can play a causal role in genetic diseases. The functional impact of CNV cannot be fully captured through linkage disequilibrium with SNPs. These observations motivate the development of statistical methods for performing direct CNV as...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Prif Awduron: Barnes, Chris, Plagnol, Vincent, Fitzgerald, Tomas, Redon, Richard, Marchini, Jonathan, Clayton, David, Hurles, Matthew E
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: 2008
Pynciau:
Mynediad Ar-lein:https://ncbi.nlm.nih.gov/pmc/articles/PMC2784596/
https://ncbi.nlm.nih.gov/pubmed/18776912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.206
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