Deep learning models achieve state-of-the art results in predicting blood glucose trajectories, with a wide range of architectures being proposed. However, the adaptation of such models in clinical practice is slow, largely due to the lack of uncertainty quantification of provided predictions. In this work, we propose to model the future glucose trajectory conditioned on the past as an infinite mixture of basis distributions (i.e., Gaussian, Laplace, etc.). This change allows us to learn the uncertainty and predict more accurately in the cases when the trajectory has a heterogeneous or multi-modal distribution. To estimate the parameters of the predictive distribution, we utilize the Transformer architecture. We empirically demonstrate the superiority of our method over existing state-of-the-art techniques both in terms of accuracy and uncertainty on the synthetic and benchmark glucose data sets.
We consider the problem of extracting joint and individual signals from multi-view data, that is data collected from different sources on matched samples. While existing methods for multi-view data decomposition explore single matching of data by samples, we focus on double-matched multi-view data (matched by both samples and source features). Our motivating example is the miRNA data collected from both primary tumor and normal tissues of the same subjects; the measurements from two tissues are thus matched both by subjects and by miRNAs. Our proposed double-matched matrix decomposition allows to simultaneously extract joint and individual signals across subjects, as well as joint and individual signals across miRNAs. Our estimation approach takes advantage of double-matching by formulating a new type of optimization problem with explicit row space and column space constraints, for which we develop an efficient iterative algorithm. Numerical studies indicate that taking advantage of double-matching leads to superior signal estimation performance compared to existing multi-view data decomposition based on single-matching. We apply our method to miRNA data as well as data from the English Premier League soccer matches, and find joint and individual multi-view signals that align with domain specific knowledge.
Large-sample data became prevalent as data acquisition became cheaper and easier. While a large sample size has theoretical advantages for many statistical methods, it presents computational challenges. Sketching, or compression, is a well-studied approach to address these issues in regression settings, but considerably less is known about its performance in classification settings. Here we consider the computational issues due to large sample size within the discriminant analysis framework. We propose a new compression approach for reducing the number of training samples for linear and quadratic discriminant analysis, in contrast to existing compression methods which focus on reducing the number of features. We support our approach with a theoretical bound on the misclassification error rate compared to the Bayes classifier. Empirical studies confirm the significant computational gains of the proposed method and its superior predictive ability compared to random sub-sampling.
We consider the two-group classification problem and propose a kernel classifier based on the optimal scoring framework. Unlike previous approaches, we provide theoretical guarantees on the expected risk consistency of the method. We also allow for feature selection by imposing structured sparsity using weighted kernels. We propose fully-automated methods for selection of all tuning parameters, and in particular adapt kernel shrinkage ideas for ridge parameter selection. Numerical studies demonstrate the superior classification performance of the proposed approach compared to existing nonparametric classifiers.
Multi-view data, that is matched sets of measurements on the same subjects, have become increasingly common with technological advances in genomics and other fields. Often, the subjects are separated into known classes, and it is of interest to find associations between the views that are related to the class membership. Existing classification methods can either be applied to each view separately, or to the concatenated matrix of all views without taking into account between-views associations. On the other hand, existing association methods can not directly incorporate class information. In this work we propose a framework for Joint Association and Classification Analysis of multi-view data (JACA). We support the methodology with theoretical guarantees for estimation consistency in high-dimensional settings, and numerical comparisons with existing methods. In addition to joint learning framework, a distinct advantage of our approach is its ability to use partial information: it can be applied both in the settings with missing class labels, and in the settings with missing subsets of views. We apply JACA to colorectal cancer data from The Cancer Genome Atlas project, and quantify the association between RNAseq and miRNA views with respect to consensus molecular subtypes of colorectal cancer.
The abundance of high-dimensional data in the modern sciences has generated tremendous interest in penalized estimators such as the lasso, scaled lasso, square-root lasso, elastic net, and many others. In this paper, we establish a general oracle inequality for prediction in high-dimensional linear regression with such methods. Since the proof relies only on convexity and continuity arguments, the result holds irrespective of the design matrix and applies to a wide range of penalized estimators. Overall, the bound demonstrates that generic estimators can provide consistent prediction with any design matrix. From a practical point of view, the bound can help to identify the potential of specific estimators, and they can help to get a sense of the prediction accuracy in a given application.
We consider the problem of high-dimensional classification between the two groups with unequal covariance matrices. Rather than estimating the full quadratic discriminant rule, we propose to perform simultaneous variable selection and linear dimension reduction on original data, with the subsequent application of quadratic discriminant analysis on the reduced space. In contrast to quadratic discriminant analysis, the proposed framework doesn't require estimation of precision matrices and scales linearly with the number of measurements, making it especially attractive for the use on high-dimensional datasets. We support the methodology with theoretical guarantees on variable selection consistency, and empirical comparison with competing approaches. We apply the method to gene expression data of breast cancer patients, and confirm the crucial importance of ESR1 gene in differentiating estrogen receptor status.
The increased availability of the multi-view data (data on the same samples from multiple sources) has led to strong interest in models based on low-rank matrix factorizations. These models represent each data view via shared and individual components, and have been successfully applied for exploratory dimension reduction, association analysis between the views, and further learning tasks such as consensus clustering. Despite these advances, there remain significant challenges in modeling partially-shared components, and identifying the number of components of each type (shared/partially-shared/individual). In this work, we formulate a novel linked component model that directly incorporates partially-shared structures. We call this model SLIDE for Structural Learning and Integrative DEcomposition of multi-view data. We prove the existence of SLIDE decomposition and explicitly characterize the identifiability conditions. The proposed model fitting and selection techniques allow for joint identification of the number of components of each type, in contrast to existing sequential approaches. In our empirical studies, SLIDE demonstrates excellent performance in both signal estimation and component selection. We further illustrate the methodology on the breast cancer data from The Cancer Genome Atlas repository.
The TREX is a recently introduced method for performing sparse high-dimensional regression. Despite its statistical promise as an alternative to the lasso, square-root lasso, and scaled lasso, the TREX is computationally challenging in that it requires solving a non-convex optimization problem. This paper shows a remarkable result: despite the non-convexity of the TREX problem, there exists a polynomial-time algorithm that is guaranteed to find the global minimum. This result adds the TREX to a very short list of non-convex optimization problems that can be globally optimized (principal components analysis being a famous example). After deriving and developing this new approach, we demonstrate that (i) the ability of the preexisting TREX heuristic to reach the global minimum is strongly dependent on the difficulty of the underlying statistical problem, (ii) the new polynomial-time algorithm for TREX permits a novel variable ranking and selection scheme, (iii) this scheme can be incorporated into a rule that controls the false discovery rate (FDR) of included features in the model. To achieve this last aim, we provide an extension of the results of Barber & Candes (2015) to establish that the knockoff filter framework can be applied to the TREX. This investigation thus provides both a rare case study of a heuristic for non-convex optimization and a novel way of exploiting non-convexity for statistical inference.
We investigate the difference between using an $\ell_1$ penalty versus an $\ell_1$ constraint in generalized eigenvalue problems, such as principal component analysis and discriminant analysis. Our main finding is that an $\ell_1$ penalty may fail to provide very sparse solutions; a severe disadvantage for variable selection that can be remedied by using an $\ell_1$ constraint. Our claims are supported both by empirical evidence and theoretical analysis. Finally, we illustrate the advantages of an $\ell_1$ constraint in the context of discriminant analysis and principal component analysis.