A carregar...

Type I error rates of rare single nucleotide variants are inflated in tests of association with non–normally distributed traits using simple linear regression methods

In this study, the effects of (a) the minor allele frequency of the single nucleotide variant (SNV), (b) the degree of departure from normality of the trait, and (c) the position of the SNVs on type I error rates were investigated in the Genetic Analysis Workshop (GAW) 19 whole exome sequence data....

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Publicado no:BMC Proc
Main Authors: Schwantes-An, Tae-Hwi, Sung, Heejong, Sabourin, Jeremy A., Justice, Cristina M., Sorant, Alexa J. M., Wilson, Alexander F.
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2016
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5133479/
https://ncbi.nlm.nih.gov/pubmed/27980666
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12919-016-0060-7
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!