Genome bioinformatic analysis of nonsynonymous SNPs

BACKGROUND: Genome-wide association studies of common diseases for common, low penetrance causal variants are underway. A proportion of these will alter protein sequences, the most common of which is the non-synonymous single nucleotide polymorphism (nsSNP). It would be an advantage if the functiona...

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Detalles Bibliográficos
Autores principales: Burke, David F, Worth, Catherine L, Priego, Eva-Maria, Cheng, Tammy, Smink, Luc J, Todd, John A, Blundell, Tom L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Methodology Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978506/
https://www.ncbi.nlm.nih.gov/pubmed/17708757
http://dx.doi.org/10.1186/1471-2105-8-301

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1978506/
https://www.ncbi.nlm.nih.gov/pubmed/17708757
http://dx.doi.org/10.1186/1471-2105-8-301

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