Genome-wide prediction of splice-modifying SNPs in human genes using a new analysis pipeline called AASsites

BACKGROUND: Some single nucleotide polymorphisms (SNPs) are known to modify the risk of developing certain diseases or the reaction to drugs. Due to next generation sequencing methods the number of known human SNPs has grown. Not all SNPs lead to a modified protein, which may be the origin of a dise...

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Detalles Bibliográficos
Autores principales: Faber, Kirsten, Glatting, Karl-Heinz, Mueller, Phillip J, Risch, Angela, Hotz-Wagenblatt, Agnes
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194194/
https://www.ncbi.nlm.nih.gov/pubmed/21992029
http://dx.doi.org/10.1186/1471-2105-12-S4-S2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3194194/
https://www.ncbi.nlm.nih.gov/pubmed/21992029
http://dx.doi.org/10.1186/1471-2105-12-S4-S2

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