VTET: a variable threshold exact test for identifying disease-associated copy number variations enriched in short genomic regions

Copy number variations (CNVs) constitute a major source of genetic variations in human populations and have been reported to be associated with complex diseases. Methods have been developed for detecting CNVs and testing CNV associations in genome-wide association studies (GWAS) based on SNP arrays....

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Detalles Bibliográficos
Autores principales: Shi, Jianxin, Yang, Xiaohong R., Caporaso, Neil E., Landi, Maria T., Li, Peng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957064/
https://www.ncbi.nlm.nih.gov/pubmed/24672538
http://dx.doi.org/10.3389/fgene.2014.00053

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3957064/
https://www.ncbi.nlm.nih.gov/pubmed/24672538
http://dx.doi.org/10.3389/fgene.2014.00053

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