Collins A, Morton N E
Human Genetics, University of Southampton, Level G, Princess Anne Hospital, Coxford Road, Southampton SO16 5YA, United Kingdom.
Proc Natl Acad Sci U S A. 1998 Feb 17;95(4):1741-5. doi: 10.1073/pnas.95.4.1741.
Allelic association provides a means to map disease genes that, in a dense map of polymorphic markers, has considerably higher resolution than linkage methods. We describe here a composite likelihood estimate of location for a disease gene against a high-resolution marker map by using allele frequencies at linked loci. Data may be family-based, as in the transmission disequilibrium test, or from a case-control study. chi2 tests, logarithm of odds, standard errors, and information weights are provided. The method is illustrated by analysis of published cystic fibrosis haplotypes, in which DeltaF508 is more accurately localized than by other association studies. This differs from current approaches by adopting a more general Malecot model for isolation by distance, where distance here is between marker and disease locus, allowance for errors in the map and model, and freedom from assumptions about demography, systematic pressures, and the ratio of physical to genetic distance. When these assumptions are introduced the number of generations since the original mutation may be estimated, but this is not required to determine location and its standard error, so that evidence from allelic association may be efficiently combined with linkage evidence to identify a region for positional cloning of a disease gene.
等位基因关联提供了一种定位疾病基因的方法,在多态性标记的密集图谱中,其分辨率比连锁方法高得多。我们在此描述了一种针对高分辨率标记图谱的疾病基因位置的复合似然估计方法,该方法通过使用连锁位点的等位基因频率来实现。数据可以基于家系,如在传递不平衡检验中,也可以来自病例对照研究。文中提供了卡方检验、优势对数、标准误差和信息权重。通过对已发表的囊性纤维化单倍型进行分析来说明该方法,在该分析中,ΔF508的定位比其他关联研究更准确。该方法与当前方法的不同之处在于,它采用了一种更通用的距离隔离Malecot模型,这里的距离是指标记与疾病位点之间的距离,考虑了图谱和模型中的误差,并且不受关于人口统计学、系统压力以及物理距离与遗传距离之比的假设的限制。当引入这些假设时,可以估计自原始突变以来的世代数,但确定位置及其标准误差并不需要这一点,因此等位基因关联的证据可以有效地与连锁证据相结合,以确定疾病基因位置克隆的区域。