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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Bibliographic Details
Main Authors: De Baets, Greet, Van Durme, Joost, Reumers, Joke, Maurer-Stroh, Sebastian, Vanhee, Peter, Dopazo, Joaquin, Schymkowitz, Joost, Rousseau, Frederic
Format: Artigo
Language:Inglês
Published: Oxford University Press 2012
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Articles
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC3245173/
https://ncbi.nlm.nih.gov/pubmed/22075996
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/nar/gkr996
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