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The power of gene-based rare variant methods to detect disease-associated variation and test hypotheses about complex disease.

Genome and exome sequencing in large cohorts enables characterization of the role of rare variation in complex diseases. Success in this endeavor, however, requires investigators to test a diverse array of genetic hypotheses which differ in the number, frequency and effect sizes of underlying causal...

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Detalhes bibliográficos
Main Authors: Loukas Moutsianas, Vineeta Agarwala, Christian Fuchsberger, Jason Flannick, Manuel A Rivas, Kyle J Gaulton, Patrick K Albers, GoT2D Consortium, Gil McVean, Michael Boehnke, David Altshuler, Mark I McCarthy
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science (PLoS) 2015-04-01
Colecção:PLoS Genetics
Acesso em linha:http://europepmc.org/articles/PMC4407972?pdf=render
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