Genome-Wide Canonical Correlation Analysis-Based Computational Methods for Mining Information from Microbiome and Gene Expression Data.

Multi-omics datasets are very high-dimensional in nature and have relatively fewer number of samples compared to the number of features. Canonical correlation analysis (CCA)-based methods are commonly used for reducing the dimensions of such multi-view (multi-omics) datasets to test the associations among the features from different views and to make them suitable for downstream analyses (classification, clustering etc.). However, most of the CCA approaches suffer from lack of interpretability and result in poor performance in the downstream analyses. Presently, there is no well-explored comparison study for CCA methods with application to multi-omics datasets (such as microbiome and gene expression datasets). In this study, we address this gap by providing a detail comparison study of three popular CCA approaches: regularized canonical correlation analysis (RCC), deep canonical correlation analysis (DCCA), and sparse canonical correlation analysis (SCCA) using a multi-omics dataset consisting of microbiome and gene expression profiles. We evaluated the methods in terms of the total correlation score, and the classification performance. We found that the SCCA provides reasonable correlation scores in the reduced space, enables interpretability, and also provides the best classification performance among the three methods.