Single nucleotide polymorphism seeking long term association with complex disease

被引:161
作者
Kirk, BW
Feinsod, M
Favis, R
Kliman, RM
Barany, F
机构
[1] Cornell Univ, Joan & Sanford I Weill Med Coll, Strang Canc Prevent Ctr, Hearst Microbiol Res Ctr,Dept Microbiol, New York, NY 10021 USA
[2] Kean Univ, Dept Biol Sci, Union, NJ 07083 USA
关键词
D O I
10.1093/nar/gkf466
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Successful investigation of commond diseases requires advances in our understanding of the organization of the genome. Linkage disequilibrium provides a theoretical basis for performing candidate gene or whole-genome association studies to analyze complex disease. However, to constructively interrogate SNPs for these studies, technologies with sufficient throughout and sensitivity are required. A plethora of suitable and reliable methods have been developed, each of which has its own unique advantage. The characteristics of the most promising genotyping and polymorphism scanning technologies are presented. These technologies are examined both in the context of complex disease investigation and in their capacity to face the unique physical and molecular challenges (allele amplification, loss of heterozygosity and stromal contamination) of solid tumor research.
引用
收藏
页码:3295 / 3311
页数:17
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