Abstract
The Umpire 2.0 R-package offers a streamlined, user-friendly workflow to simulate complex, heterogeneous, mixed-type data with known subgroup identities, dichotomous outcomes, and time-to-event data, while providing ample opportunities for fine-tuning and flexibility. Here, we describe how we have expanded the core Umpire 1.0 R-package, developed to simulate gene expression data, to generate clinically realistic, mixed-type data for use in evaluating unsupervised and supervised machine learning (ML) methods. As the availability of large-scale clinical data for ML has increased, clinical data has posed unique challenges, including widely variable size, individual biological heterogeneity, data collection and measurement noise, and mixed data types. Developing and validating ML methods for clinical data requires data sets with known ground truth, generated from simulation. Umpire 2.0 addresses challenges to simulating realistic clinical data by providing the user a series of modules to generate survival parameters and subgroups, apply meaningful additive noise, and discretize to single or mixed data types. Umpire 2.0 provides broad functionality across sample sizes, feature spaces, and data types, allowing the user to simulate correlated, heterogeneous, binary, continuous, categorical, or mixed type data from the scale of a small clinical trial to data on thousands of patients drawn from electronic health records. The user may generate elaborate simulations by varying parameters in order to compare algorithms or interrogate operating characteristics of an algorithm in both supervised and unsupervised ML.
Funder
National Center for Advancing Translational Sciences
National Cancer Institute
Subject
General Pharmacology, Toxicology and Pharmaceutics,General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine
Cited by
3 articles.
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