Article
Disease association tests by inferring ancestral haplotypes using a hidden markov model.
Bioinformatics (Oxford, England) - 1 Apr 2008
Su Shu-Yi, Balding David J, Coin Lachlan J M
Abstract excerpt
MOTIVATION: Most genome-wide association studies rely on single nucleotide polymorphism (SNP) analyses to identify causal loci. The increased stringency required for genome-wide analyses (with per-SNP significance threshold typically approximately 10(-7)) means that many real signals will be miss...
Topics
- Algorithms
- Biological Evolution
- Chromosome Mapping
- Computer Simulation
- Genetic Predisposition to Disease
- Haplotypes
- Markov Chains
- Models, Genetic
- Models, Statistical
- Pattern Recognition, Automated
