A Robust GWSS Method to Simultaneously Detect Rare and Common Variants for Complex Disease

The rapid advances in sequencing technologies and the resulting next-generation sequencing data provide the opportunity to detect disease-associated variants with a better solution, in particular for low-frequency variants. Although both common and rare variants might exert their independent effects...

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Detalles Bibliográficos
Autores principales: Kao, Chung-Feng, Liu, Jia-Rou, Hung, Hung, Kuo, Po-Hsiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399906/
https://www.ncbi.nlm.nih.gov/pubmed/25880329
http://dx.doi.org/10.1371/journal.pone.0120873

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4399906/
https://www.ncbi.nlm.nih.gov/pubmed/25880329
http://dx.doi.org/10.1371/journal.pone.0120873

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