Meuwissen Theo H E, Goddard Mike E
IHA, Norwegian Academy of Life Sciences, 1432 As, Norway.
Genetics. 2007 Aug;176(4):2551-60. doi: 10.1534/genetics.107.070953. Epub 2007 Jun 11.
A novel multipoint method, based on an approximate coalescence approach, to analyze multiple linked markers is presented. Unlike other approximate coalescence methods, it considers all markers simultaneously but only two haplotypes at a time. We demonstrate the use of this method for linkage disequilibrium (LD) mapping of QTL and estimation of effective population size. The method estimates identity-by-descent (IBD) probabilities between pairs of marker haplotypes. Both LD and combined linkage and LD mapping rely on such IBD probabilities. The method is approximate in that it considers only the information on a pair of haplotypes, whereas a full modeling of the coalescence process would simultaneously consider all haplotypes. However, full coalescence modeling is computationally feasible only for few linked markers. Using simulations of the coalescence process, the method is shown to give almost unbiased estimates of the effective population size. Compared to direct marker and haplotype association analyses, IBD-based QTL mapping showed clearly a higher power to detect a QTL and a more realistic confidence interval for its position. The modeling of LD could be extended to estimate other LD-related parameters such as recombination rates.
本文提出了一种基于近似合并方法的新型多点方法,用于分析多个连锁标记。与其他近似合并方法不同,该方法同时考虑所有标记,但每次仅考虑两个单倍型。我们展示了该方法在数量性状基因座(QTL)的连锁不平衡(LD)作图和有效种群大小估计中的应用。该方法估计标记单倍型对之间的同源系数(IBD)概率。LD作图以及联合连锁和LD作图均依赖于此类IBD概率。该方法是近似的,因为它仅考虑一对单倍型的信息,而合并过程的完整建模会同时考虑所有单倍型。然而,完整的合并建模仅对少数连锁标记在计算上是可行的。通过合并过程的模拟,该方法被证明能给出几乎无偏的有效种群大小估计。与直接的标记和单倍型关联分析相比,基于IBD的QTL作图在检测QTL方面具有更高的功效,并且其位置的置信区间更符合实际情况。LD的建模可以扩展到估计其他与LD相关的参数,如重组率。