Article
Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies.
Genome research - 1 Aug 2004
Halldórsson Bjarni V, Bafna Vineet, Lippert Ross, Schwartz Russell, De La Vega Francisco M, Clark Andrew G, Istrail Sorin
Abstract excerpt
It is widely hoped that the study of sequence variation in the human genome will provide a means of elucidating the genetic component of complex diseases and variable drug responses. A major stumbling block to the successful design and execution of genome-wide disease association studies using si...
Topics
- Algorithms
- Chromosomes, Human, Pair 22
- Genetic Variation
- Haplotypes
- Humans
- Linkage Disequilibrium
- Models, Genetic
- Polymorphism, Single Nucleotide
- Research Design
