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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...

Disgrifiad llawn

Wedi'i Gadw mewn:
Manylion Llyfryddiaeth
Cyhoeddwyd yn:Eur J Hum Genet
Prif Awduron: Peloso, Gina M, Rader, Daniel J, Gabriel, Stacey, Kathiresan, Sekar, Daly, Mark J, Neale, Benjamin M
Fformat: Artigo
Iaith:Inglês
Cyhoeddwyd: Nature Publishing Group 2016
Pynciau:
Mynediad Ar-lein: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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