Article
Single-nucleotide polymorphism genotyping for disease association studies.
Methods in molecular medicine - 1 Jan 2005
Fornage Myriam, Doris Peter A
Abstract excerpt
The Human Genome Project has led to the discovery of millions of DNA sequence variants in the human genome. The majority of these variants are single-nucleotide polymorphisms (SNPs). Availability of an ultra-high-density SNP map, combined with improvement in genotyping technologies and efficient analytical approaches, opens the possibility of fulfilling the promise of SNP association studies to reveal why some...
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