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Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies

We propose in this paper a unified approach for testing the association between rare variants and phenotypes in sequencing association studies. This approach maximizes power by adaptively using the data to optimally combine the burden test and the nonburden sequence kernel association test (SKAT). B...

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Main Authors: Lee, Seunggeun, Emond, Mary J., Bamshad, Michael J., Barnes, Kathleen C., Rieder, Mark J., Nickerson, Deborah A., Christiani, David C., Wurfel, Mark M., Lin, Xihong
Format: Artigo
Jezik:Inglês
Izdano: Elsevier 2012
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC3415556/
https://ncbi.nlm.nih.gov/pubmed/22863193
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2012.06.007
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