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Phenotypic extremes in rare variant study designs

Currently, next-generation sequencing studies aim to identify rare and low-frequency variation that may contribute to disease. For a given effect size, as the allele frequency decreases, the power to detect genes or variants of interest also decreases. Although many methods have been proposed for th...

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Bibliografske podrobnosti
izdano v:Eur J Hum Genet
Main Authors: Peloso, Gina M, Rader, Daniel J, Gabriel, Stacey, Kathiresan, Sekar, Daly, Mark J, Neale, Benjamin M
Format: Artigo
Jezik:Inglês
Izdano: Nature Publishing Group 2016
Teme:
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC4867440/
https://ncbi.nlm.nih.gov/pubmed/26350511
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2015.197
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