SNPeffect 4.0: on-line prediction of molecular and structural effects of protein-coding variants

Single nucleotide variants (SNVs) are, together with copy number variation, the primary source of variation in the human genome and are associated with phenotypic variation such as altered response to drug treatment and susceptibility to disease. Linking structural effects of non-synonymous SNVs to...

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Detalles Bibliográficos
Autores principales: De Baets, Greet, Van Durme, Joost, Reumers, Joke, Maurer-Stroh, Sebastian, Vanhee, Peter, Dopazo, Joaquin, Schymkowitz, Joost, Rousseau, Frederic
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245173/
https://www.ncbi.nlm.nih.gov/pubmed/22075996
http://dx.doi.org/10.1093/nar/gkr996

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3245173/
https://www.ncbi.nlm.nih.gov/pubmed/22075996
http://dx.doi.org/10.1093/nar/gkr996

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