Sung Yun Ju, Thompson Elizabeth A, Wijsman Ellen M
Division of Medical Genetics, Department of Medicine, University of Washington, Seattle, WA 98195-7720, USA.
Genet Epidemiol. 2007 Feb;31(2):103-14. doi: 10.1002/gepi.20194.
We describe a new program lm_twoqtl, part of the MORGAN package, for parametric linkage analysis with a quantitative trait locus (QTL) model having one or two QTLs and a polygenic component, which models additional familial correlation from other unlinked QTLs. The program has no restriction on number of markers or complexity of pedigrees, facilitating use of more complex models with general pedigrees. This is the first available program that can handle a model with both two QTLs and a polygenic component. Competing programs use only simpler models: one QTL, one QTL plus a polygenic component, or variance components (VC). Use of simple models when they are incorrect, as for complex traits that are influenced by multiple genes, can bias estimates of QTL location or reduce power to detect linkage. We compute the likelihood with Markov Chain Monte Carlo (MCMC) realization of segregation indicators at the hypothesized QTL locations conditional on marker data, summation over phased multilocus genotypes of founders, and peeling of the polygenic component. Simulated examples, with various sized pedigrees, show that two-QTL analysis correctly identifies the location of both QTLs, even when they are closely linked, whereas other analyses, including the VC approach, fail to identify the location of QTLs with modest contribution. Our examples illustrate the advantage of parametric linkage analysis with two QTLs, which provides higher power for linkage detection and better localization than use of simpler models.
我们描述了一个新程序lm_twoqtl,它是MORGAN软件包的一部分,用于具有一个或两个数量性状基因座(QTL)和一个多基因成分的QTL模型的参数连锁分析,该模型可对来自其他不连锁QTL的额外家族相关性进行建模。该程序对标记数量或系谱复杂性没有限制,便于在一般系谱中使用更复杂的模型。这是首个可处理同时包含两个QTL和一个多基因成分模型的程序。与之竞争的程序仅使用更简单的模型:一个QTL、一个QTL加一个多基因成分或方差成分(VC)。对于受多个基因影响的复杂性状,在模型不正确时使用简单模型可能会使QTL位置的估计产生偏差或降低检测连锁的能力。我们通过在假设的QTL位置基于标记数据对分离指标进行马尔可夫链蒙特卡罗(MCMC)实现、对奠基者的分阶段多位点基因型求和以及对多基因成分进行剥离来计算似然性。具有各种规模系谱的模拟示例表明,双QTL分析能够正确识别两个QTL的位置,即使它们紧密连锁,而其他分析方法,包括VC方法,在QTL贡献较小时无法识别其位置。我们的示例说明了使用两个QTL进行参数连锁分析的优势,与使用更简单模型相比,它在连锁检测方面具有更高的功效和更好的定位效果。