A computational framework discovers new copy number variants with functional importance.

Structural variants which cause changes in copy numbers constitute an important component of genomic variability. They account for 0.7% of genomic differences in two individual genomes, of which copy number variants (CNVs) are the largest component. A recent population-based CNV study revealed the n...

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Detalhes bibliográficos

Principais autores:	Samprit Banerjee, Derek Oldridge, Maria Poptsova, Wasay M Hussain, Dimple Chakravarty, Francesca Demichelis
Formato:	Artigo
Idioma:	Inglês
Publicado em:	Public Library of Science (PLoS) 2011-03-01
coleção:	PLoS ONE
Acesso em linha:	http://europepmc.org/articles/PMC3066184?pdf=render
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