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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...
| Autores principales: | , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2008
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| Materias: | |
| 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 |