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Bivariate logistic Bayesian LASSO for detecting rare haplotype association with two correlated phenotypes

机译:用于检测稀有单倍型与两种相关表型的稀有单倍型关联的双偏见物流贝塞

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Abstract In genetic association studies, joint modeling of related traits/phenotypes can utilize the correlation between them and thereby provide more power and uncover additional information about genetic etiology. Moreover, detecting rare genetic variants are of current scientific interest as a key to missing heritability. Logistic Bayesian LASSO (LBL) has been proposed recently to detect rare haplotype variants using case‐control data, that is, a single binary phenotype. As there is currently no haplotype association method that can handle multiple binary phenotypes, we extend LBL to fill this gap. We develop a bivariate model by using a latent variable to induce correlation between the two outcomes. We carry out extensive simulations to investigate the bivariate LBL and compare with the univariate LBL. The bivariate LBL performs better or similar to the univariate LBL in most settings. It has the highest gain in power when a haplotype is associated with both traits and it affects at least one trait in a direction opposite to the direction of the correlation between the traits. We analyze two data sets—Genetic Analysis Workshop 19 sequence data on systolic and diastolic blood pressures and a genome‐wide association data set on lung cancer and smoking and detect several associated rare haplotypes.
机译:摘要在遗传关联研究中,相关性状/表型的联合建模可以利用它们之间的相关性,从而提供更多的功率并揭示有关遗传病因的额外信息。此外,检测稀有遗传变异是当前科学兴趣的关键是遗漏的关键。最近已经提出了Logistic Bayesian套索(LBL)以检测使用病例控制数据的稀有单倍型变体,即单个二进制表型。由于目前没有可以处理多个二进制表型的单倍型关联方法,我们将LBL扩展以填补这种差距。我们通过使用潜在的变量来开发一项双变量模型,以引起两种结果之间的相关性。我们开展了广泛的模拟,以调查双变量LBL并与单变量LBL进行比较。在大多数设置中,Bivariate Lbl执行与单变量LBL更好或类似。当单倍型与两个特征相关联时,它具有最高的功率增益,并且它在与特征之间的相关方向相反的方向上影响至少一个特征。我们分析了两种数据集遗传分析研讨会19序列数据上的收缩和舒张血压和肺癌的基因组关联数据,并检测了几种相关的罕见单倍型。

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