Exhaustive prediction of disease susceptibility to coding base changes in the human genome

BACKGROUND: Single Nucleotide Polymorphisms (SNPs) are the most abundant form of genomic variation and can cause phenotypic differences between individuals, including diseases. Bases are subject to various levels of selection pressure, reflected in their inter-species conservation. RESULTS: We propo...

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Detalles Bibliográficos
Autores principales: Kulkarni, Vinayak, Errami, Mounir, Barber, Robert, Garner, Harold R
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Proceedings
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537574/
https://www.ncbi.nlm.nih.gov/pubmed/18793467
http://dx.doi.org/10.1186/1471-2105-9-S9-S3

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2537574/
https://www.ncbi.nlm.nih.gov/pubmed/18793467
http://dx.doi.org/10.1186/1471-2105-9-S9-S3

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