Advantage of Using Allele-Specific Copy Numbers When Testing for Association in Regions with Common Copy Number Variants

Copy number variants (CNV) can be called from SNP-arrays; however, few studies have attempted to combine both CNV and SNP calls to test for association with complex diseases. Even when SNPs are located within CNVs, two separate association analyses are necessary, to compare the distribution of bi-al...

Descripción completa

Detalles Bibliográficos
Autores principales: Marenne, Gaëlle, Chanock, Stephen J., Malats, Núria, Génin, Emmanuelle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769257/
https://www.ncbi.nlm.nih.gov/pubmed/24040408
http://dx.doi.org/10.1371/journal.pone.0075350

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3769257/
https://www.ncbi.nlm.nih.gov/pubmed/24040408
http://dx.doi.org/10.1371/journal.pone.0075350

Ejemplares similares