MEQMMLJun 26, 2016

Discriminating sample groups with multi-way data

arXiv:1606.08046v116 citationsHas Code
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This work addresses the need for better classification methods in biomedical research where data are multi-dimensional, offering incremental improvements for researchers analyzing complex datasets like brain metabolites or gene expression time-courses.

The authors tackled the problem of classifying high-dimensional multi-way data, such as metabolite or gene expression measurements across multiple dimensions, by proposing a framework that extends linear classifiers like SVM and DWD with low-rank coefficient factorization, resulting in improved performance and simplified interpretation over naive full-rank methods.

High-dimensional linear classifiers, such as the support vector machine (SVM) and distance weighted discrimination (DWD), are commonly used in biomedical research to distinguish groups of subjects based on a large number of features. However, their use is limited to applications where a single vector of features is measured for each subject. In practice data are often multi-way, or measured over multiple dimensions. For example, metabolite abundance may be measured over multiple regions or tissues, or gene expression may be measured over multiple time points, for the same subjects. We propose a framework for linear classification of high-dimensional multi-way data, in which coefficients can be factorized into weights that are specific to each dimension. More generally, the coefficients for each measurement in a multi-way dataset are assumed to have low-rank structure. This framework extends existing classification techniques, and we have implemented multi-way versions of SVM and DWD. We describe informative simulation results, and apply multi-way DWD to data for two very different clinical research studies. The first study uses metabolite magnetic resonance spectroscopy data over multiple brain regions to compare patients with and without spinocerebellar ataxia, the second uses publicly available gene expression time-course data to compare treatment responses for patients with multiple sclerosis. Our method improves performance and simplifies interpretation over naive applications of full rank linear classification to multi-way data. An R package is available at https://github.com/lockEF/MultiwayClassification .

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