Stepwise Model Selection for Sequence Prediction via Deep Kernel Learning

An essential problem in automated machine learning (AutoML) is that of model selection. A unique challenge in the sequential setting is the fact that the optimal model itself may vary over time, depending on the distribution of features and labels available up to each point in time. In this paper, we propose a novel Bayesian optimization (BO) algorithm to tackle the challenge of model selection in this setting. This is accomplished by treating the performance at each time step as its own black-box function. In order to solve the resulting multiple black-box function optimization problem jointly and efficiently, we exploit potential correlations among black-box functions using deep kernel learning (DKL). To the best of our knowledge, we are the first to formulate the problem of stepwise model selection (SMS) for sequence prediction, and to design and demonstrate an efficient joint-learning algorithm for this purpose. Using multiple real-world datasets, we verify that our proposed method outperforms both standard BO and multi-objective BO algorithms on a variety of sequence prediction tasks.

Learning Overlapping Representations for the Estimation of Individualized Treatment Effects

The choice of making an intervention depends on its potential benefit or harm in comparison to alternatives. Estimating the likely outcome of alternatives from observational data is a challenging problem as all outcomes are never observed, and selection bias precludes the direct comparison of differently intervened groups. Despite their empirical success, we show that algorithms that learn domain-invariant representations of inputs (on which to make predictions) are often inappropriate, and develop generalization bounds that demonstrate the dependence on domain overlap and highlight the need for invertible latent maps. Based on these results, we develop a deep kernel regression algorithm and posterior regularization framework that substantially outperforms the state-of-the-art on a variety of benchmarks data sets.

Target-Embedding Autoencoders for Supervised Representation Learning

Autoencoder-based learning has emerged as a staple for disciplining representations in unsupervised and semi-supervised settings. This paper analyzes a framework for improving generalization in a purely supervised setting, where the target space is high-dimensional. We motivate and formalize the general framework of target-embedding autoencoders (TEA) for supervised prediction, learning intermediate latent representations jointly optimized to be both predictable from features as well as predictive of targets---encoding the prior that variations in targets are driven by a compact set of underlying factors. As our theoretical contribution, we provide a guarantee of generalization for linear TEAs by demonstrating uniform stability, interpreting the benefit of the auxiliary reconstruction task as a form of regularization. As our empirical contribution, we extend validation of this approach beyond existing static classification applications to multivariate sequence forecasting, verifying their advantage on both linear and nonlinear recurrent architectures---thereby underscoring the further generality of this framework beyond feedforward instantiations.

Learning Dynamic and Personalized Comorbidity Networks from Event Data using Deep Diffusion Processes

Comorbid diseases co-occur and progress via complex temporal patterns that vary among individuals. In electronic health records we can observe the different diseases a patient has, but can only infer the temporal relationship between each co-morbid condition. Learning such temporal patterns from event data is crucial for understanding disease pathology and predicting prognoses. To this end, we develop deep diffusion processes (DDP) to model "dynamic comorbidity networks", i.e., the temporal relationships between comorbid disease onsets expressed through a dynamic graph. A DDP comprises events modelled as a multi-dimensional point process, with an intensity function parameterized by the edges of a dynamic weighted graph. The graph structure is modulated by a neural network that maps patient history to edge weights, enabling rich temporal representations for disease trajectories. The DDP parameters decouple into clinically meaningful components, which enables serving the dual purpose of accurate risk prediction and intelligible representation of disease pathology. We illustrate these features in experiments using cancer registry data.

Contextual Constrained Learning for Dose-Finding Clinical Trials

Clinical trials in the medical domain are constrained by budgets. The number of patients that can be recruited is therefore limited. When a patient population is heterogeneous, this creates difficulties in learning subgroup specific responses to a particular drug and especially for a variety of dosages. In addition, patient recruitment can be difficult by the fact that clinical trials do not aim to provide a benefit to any given patient in the trial. In this paper, we propose C3T-Budget, a contextual constrained clinical trial algorithm for dose-finding under both budget and safety constraints. The algorithm aims to maximize drug efficacy within the clinical trial while also learning about the drug being tested. C3T-Budget recruits patients with consideration of the remaining budget, the remaining time, and the characteristics of each group, such as the population distribution, estimated expected efficacy, and estimation credibility. In addition, the algorithm aims to avoid unsafe dosages. These characteristics are further illustrated in a simulated clinical trial study, which corroborates the theoretical analysis and demonstrates an efficient budget usage as well as a balanced learning-treatment trade-off.

A Bayesian Approach to Modelling Longitudinal Data in Electronic Health Records

Analyzing electronic health records (EHR) poses significant challenges because often few samples are available describing a patient's health and, when available, their information content is highly diverse. The problem we consider is how to integrate sparsely sampled longitudinal data, missing measurements informative of the underlying health status and fixed demographic information to produce estimated survival distributions updated through a patient's follow up. We propose a nonparametric probabilistic model that generates survival trajectories from an ensemble of Bayesian trees that learns variable interactions over time without specifying beforehand the longitudinal process. We show performance improvements on Primary Biliary Cirrhosis patient data.

Improving Model Robustness Using Causal Knowledge

For decades, researchers in fields, such as the natural and social sciences, have been verifying causal relationships and investigating hypotheses that are now well-established or understood as truth. These causal mechanisms are properties of the natural world, and thus are invariant conditions regardless of the collection domain or environment. We show in this paper how prior knowledge in the form of a causal graph can be utilized to guide model selection, i.e., to identify from a set of trained networks the models that are the most robust and invariant to unseen domains. Our method incorporates prior knowledge (which can be incomplete) as a Structural Causal Model (SCM) and calculates a score based on the likelihood of the SCM given the target predictions of a candidate model and the provided input variables. We show on both publicly available and synthetic datasets that our method is able to identify more robust models in terms of generalizability to unseen out-of-distribution test examples and domains where covariates have shifted.