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Incorporating predicted functions of nonsynonymous variants into gene-based analysis of exome sequencing data: a comparative study

Next-generation sequencing has opened up new avenues for the genetic study of complex traits. However, because of the small number of observations for any given rare allele and high sequencing error, it is a challenge to identify functional rare variants associated with the phenotype of interest. Re...

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Detalles Bibliográficos
Autores principales: Wei, Peng, Liu, Xiaoming, Fu, Yun-Xin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3287855/
https://www.ncbi.nlm.nih.gov/pubmed/22373178
http://dx.doi.org/10.1186/1753-6561-5-S9-S20