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Current analysis platforms and methods for detecting copy number variation

Copy number variation (CNV), generated through duplication or deletion events that affect one or more loci, is widespread in the human genomes and is often associated with functional consequences that may include changes in gene expression levels or fusion of genes. Genome-wide association studies i...

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Detalhes bibliográficos
Main Authors: Li, Wenli, Olivier, Michael
Formato: Artigo
Idioma:Inglês
Publicado em: American Physiological Society 2013
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3544484/
https://ncbi.nlm.nih.gov/pubmed/23132758
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1152/physiolgenomics.00082.2012
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