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引用次数: 0
摘要
在一些生物医学领域,数据越来越多地采用多向阵列或张量的形式。这种张量通常观察不完全。例如,在微生物组纵向研究中,有几个研究对象的几个时间点缺失。关于张量缺失数据估算的文献越来越多。然而,现有方法只给出了缺失值的点估计,却没有捕捉到不确定性。我们在一个灵活的贝叶斯框架中提出了一种张量多重估算方法,它能为缺失条目提供真实的模拟值,并能在后续分析中传播不确定性。我们的模型采用了高效且广泛适用的共轭先验,用于 CANDECOMP/PARAFAC (CP) 因子分解,具有可分离的残差协方差结构。对于张量的单个条目或整个纤维缺失的情况,这种方法在估算精度和不确定性校准方面都表现良好。在两个微生物组应用中,该方法被证明能准确捕捉缺失时间点上完整微生物组剖面的不确定性,并用于推断种群的物种多样性趋势。执行多重估算方法的 R 代码文档见 https://github.com/lockEF/MultiwayImputation 。
BAMITA: Bayesian Multiple Imputation for Tensor Arrays.
Data increasingly take the form of a multi-way array, or tensor, in several biomedical domains. Such tensors are often incompletely observed. For example, we are motivated by longitudinal microbiome studies in which several timepoints are missing for several subjects. There is a growing literature on missing data imputation for tensors. However, existing methods give a point estimate for missing values without capturing uncertainty. We propose a multiple imputation approach for tensors in a flexible Bayesian framework, that yields realistic simulated values for missing entries and can propagate uncertainty through subsequent analyses. Our model uses efficient and widely applicable conjugate priors for a CANDECOMP/PARAFAC (CP) factorization, with a separable residual covariance structure. This approach is shown to perform well with respect to both imputation accuracy and uncertainty calibration, for scenarios in which either single entries or entire fibers of the tensor are missing. For two microbiome applications, it is shown to accurately capture uncertainty in the full microbiome profile at missing timepoints and used to infer trends in species diversity for the population. Documented R code to perform our multiple imputation approach is available at https://github.com/lockEF/MultiwayImputation.