Nielsen D M, Weir B S
Program in Statistical Genetics, Department of Statistics, North Carolina State University, Raleigh, North Carolina 27695-7566, USA.
Theor Popul Biol. 2001 Nov;60(3):253-63. doi: 10.1006/tpbi.2001.1539.
There is great expectation that the levels of association found between genetic markers and disease status will play a role in the location of disease genes. This expectation follows from regarding association as being proportional to linkage disequilibrium and therefore inversely related to recombination value. For disease genes with more than two alleles, the association measure is instead a weighted average of linkage disequilibria, with the weights depending on allele frequencies and genotype susceptibilities at the disease loci. There is no longer a simple relationship, even in expectation, with recombination. We adopt a general framework to examine association mapping methods which helps to clarify the nature of case-control and transmission/disequilibrium-type tests and reveals the relationship between measures of association and coefficients of linkage disequilibrium. In particular, we can show the consequences of additive and nonadditive effects at the trait locus on the behavior of these tests. These concepts have a natural extension to marker haplotypes. The association of two-locus marker haplotypes with disease phenotype depends on a weighted average of three-locus disequilibria (two markers with each disease locus). It is likely that these two-marker analyses will provide additional information in association mapping studies.
人们寄予厚望的是,在基因标记与疾病状态之间发现的关联水平将在疾病基因定位中发挥作用。这种期望源于将关联视为与连锁不平衡成正比,因此与重组值成反比。对于具有两个以上等位基因的疾病基因,关联度量反而为连锁不平衡的加权平均值,权重取决于疾病位点的等位基因频率和基因型易感性。即使在预期情况下,与重组也不再存在简单关系。我们采用一个通用框架来检验关联定位方法,这有助于阐明病例对照和传递/不平衡类型检验的本质,并揭示关联度量与连锁不平衡系数之间的关系。特别是,我们可以展示性状位点的加性和非加性效应对这些检验行为的影响。这些概念自然地扩展到标记单倍型。双位点标记单倍型与疾病表型的关联取决于三位点不平衡(两个标记与每个疾病位点)的加权平均值。很可能这些双标记分析将在关联定位研究中提供额外信息。