We propose an approach termed "qDAGx" for Bayesian covariate-dependent quantile directed acyclic graphs (DAGs) where these DAGs are individualized, in the sense that they depend on individual-specific covariates. A key distinguishing feature of the proposed approach is that the individualized DAG structure can be uniquely identified at any given quantile, based on purely observational data without strong assumptions such as a known topological ordering. For scaling the proposed method to a large number of variables and covariates, we propose for the model parameters a novel parameter expanded horseshoe prior that affords a number of attractive theoretical and computational benefits to our approach. By modeling the conditional quantiles, qDAGx overcomes the common limitations of mean regression for DAGs, which can be sensitive to the choice of likelihood, e.g., an assumption of multivariate normality, as well as to the choice of priors. We demonstrate the performance of qDAGx through extensive numerical simulations and via an application in precision medicine by inferring patient-specific protein--protein interaction networks in lung cancer.
翻译:我们提出一种方法,即“QDAGx”方法,用于巴伊西亚共分数依赖孔径的圆形图(DAGs),即这些DAG是个别化的,即取决于个别的共分数。拟议方法的一个重要区别特征是,在任何特定孔径上,单个化的DAG结构可以根据纯粹的观察数据而单独确定,而没有已知的地形顺序等强有力的假设。为了将拟议方法推广到大量变量和共分数,我们建议模型参数采用新的参数,扩大马蹄杆,在之前为我们的方法提供若干有吸引力的理论和计算效益。通过模拟有条件的孔径,QDAGs克服了对DAGs平均回归的共同限制,这些限制可能敏感于可能性的选择,例如多变法性正常性的假设,以及先前的选择。我们通过广泛的数字模拟和通过推断特定病人蛋白质相互作用网络在肺癌中应用精确医学,来证明qDAGx的表现。