Linkage-disequilibrium mapping of disease genes by reconstruction of ancestral haplotypes in founder populations

被引:87
|
作者
Service, SK
Lang, DWT
Freimer, NB [1 ]
Sandkuijl, LA
机构
[1] Univ Calif San Francisco, Neurogenet Lab, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Ctr Neurobiol & Psychiat, Dept Psychiat, San Francisco, CA 94143 USA
[3] AT&T Bell Labs, Lucent Technol, Murray Hill, NJ 07974 USA
[4] Erasmus Univ, Dept Clin Genet, NL-3000 DR Rotterdam, Netherlands
[5] Leiden Univ, Dept Human Genet, NL-2300 RA Leiden, Netherlands
[6] Univ Groningen, Dept Med Genet, Groningen, Netherlands
关键词
D O I
10.1086/302398
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Linkage disequilibrium (LD) mapping may be a powerful means for genome screening to identify susceptibility loci for common diseases. Anew statistical approach for detection of LD around a disease gene is presented here. This method compares the distribution of haplotypes in affected individuals versus that expected for individuals descended from a common ancestor who carried a mutation of the disease gene. Simulations demonstrate that this method, which we term "ancestral haplotype reconstruction" (AHR), should be powerful for genome screening of phenotypes characterized by a high degree of etiologic heterogeneity, even with currently available marker maps; AHR is best suited to application in isolated populations where affected individuals are relatively recently descended (<similar to 25 generations) from a common disease mutation-bearing founder.
引用
收藏
页码:1728 / 1738
页数:11
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