Biswas Swati, Papachristou Charalampos
Department of Mathematical Sciences, FO 35, University of Texas at Dallas, 800 West Campbell Road,Richardson, TX 75080, USA.
Department of Mathematics, Physics, and Statistics, University of the Sciences in Philadelphia, 600 South 43rd Street, Philadelphia, PA 19104, USA.
BMC Proc. 2014 Jun 17;8(Suppl 1):S54. doi: 10.1186/1753-6561-8-S1-S54. eCollection 2014.
It has been hypothesized that rare variants may hold the key to unraveling the genetic transmission mechanism of many common complex traits. Currently, there is a dearth of statistical methods that are powerful enough to detect association with rare haplotypes. One of the recently proposed methods is logistic Bayesian LASSO for case-control data. By penalizing the regression coefficients through appropriate priors, logistic Bayesian LASSO weeds out the unassociated haplotypes, making it possible for the associated rare haplotypes to be detected with higher powers. We used the Genetic Analysis Workshop 18 simulated data to evaluate the behavior of logistic Bayesian LASSO in terms of its power and type I error under a complex disease model. We obtained knowledge of the simulation model, including the locations of the functional variants, and we chose to focus on two genomic regions in the MAP4 gene on chromosome 3. The sample size was 142 individuals and there were 200 replicates. Despite the small sample size, logistic Bayesian LASSO showed high power to detect two haplotypes containing functional variants in these regions while maintaining low type I errors. At the same time, a commonly used approach for haplotype association implemented in the software hapassoc failed to converge because of the presence of rare haplotypes. Thus, we conclude that logistic Bayesian LASSO can play an important role in the search for rare haplotypes.
有假设认为,罕见变异可能是解开许多常见复杂性状遗传传递机制的关键。目前,缺乏足够强大的统计方法来检测与罕见单倍型的关联。最近提出的方法之一是用于病例对照数据的逻辑贝叶斯套索法。通过适当的先验对回归系数进行惩罚,逻辑贝叶斯套索法排除了不相关的单倍型,使得有可能以更高的效能检测出相关的罕见单倍型。我们使用遗传分析研讨会18的模拟数据,在复杂疾病模型下评估逻辑贝叶斯套索法在效能和I型错误方面的表现。我们了解了模拟模型,包括功能变异的位置,并选择聚焦于3号染色体上MAP4基因的两个基因组区域。样本量为142个个体,有200次重复。尽管样本量较小,但逻辑贝叶斯套索法在检测这些区域中包含功能变异的两个单倍型时显示出高效能,同时保持低I型错误。与此同时,软件haplassoc中实现的一种常用单倍型关联方法由于存在罕见单倍型而未能收敛。因此,我们得出结论,逻辑贝叶斯套索法在寻找罕见单倍型方面可以发挥重要作用。