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VarMod: modelling the functional effects of non-synonymous variants

Unravelling the genotype–phenotype relationship in humans remains a challenging task in genomics studies. Recent advances in sequencing technologies mean there are now thousands of sequenced human genomes, revealing millions of single nucleotide variants (SNVs). For non-synonymous SNVs present in pr...

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Detalles Bibliográficos
Autores principales:	Pappalardo, Morena, Wass, Mark N.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Oxford University Press 2014
Materias:	Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086131/ https://www.ncbi.nlm.nih.gov/pubmed/24906884 http://dx.doi.org/10.1093/nar/gku483

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