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Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

Deep sequencing will soon generate comprehensive sequence information in large disease samples. Although the power to detect association with an individual rare variant is limited, pooling variants by gene or pathway into a composite test provides an alternative strategy for identifying susceptibili...

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Détails bibliographiques
Auteurs principaux: Price, Alkes L., Kryukov, Gregory V., de Bakker, Paul I.W., Purcell, Shaun M., Staples, Jeff, Wei, Lee-Jen, Sunyaev, Shamil R.
Format: Artigo
Langue:Inglês
Publié: Elsevier 2010
Sujets:
Accès en ligne:https://ncbi.nlm.nih.gov/pmc/articles/PMC3032073/
https://ncbi.nlm.nih.gov/pubmed/20471002
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2010.04.005
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