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Statistical tests for detecting rare variants using variance-stabilizing transformations

Next generation sequencing holds great promise for detecting rare variants underlying complex human traits. Due to their extremely low allele frequencies, the normality approximation for a proportion no longer works well. The Fisher’s exact method appears to be suitable but it is conservative. We in...

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Detalles Bibliográficos
Autores principales: Wang, Kai, Fingert, John H.
Formato: Artigo
Lenguaje:Inglês
Publicado: 2012
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Acceso en línea:https://ncbi.nlm.nih.gov/pmc/articles/PMC3418475/
https://ncbi.nlm.nih.gov/pubmed/22724536
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/j.1469-1809.2012.00718.x
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