Weighted pedigree-based statistics for testing the association of rare variants

BACKGROUND: With the advent of next-generation sequencing (NGS) technologies, researchers are now generating a deluge of data on high dimensional genomic variations, whose analysis is likely to reveal rare variants involved in the complex etiology of disease. Standing in the way of such discoveries,...

Descripción completa

Detalles Bibliográficos
Autores principales: Shugart, Yin Yao, Zhu, Yun, Guo, Wei, Xiong, Momiao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827928/
https://www.ncbi.nlm.nih.gov/pubmed/23176082
http://dx.doi.org/10.1186/1471-2164-13-667

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3827928/
https://www.ncbi.nlm.nih.gov/pubmed/23176082
http://dx.doi.org/10.1186/1471-2164-13-667

Ejemplares similares