SDGCCA: Supervised Deep Generalized Canonical Correlation Analysis for Multi-omics Integration

TL;DR

SDGCCA is a novel deep learning method that integrates multi-omics data to improve phenotype classification and biomarker discovery by modeling complex nonlinear correlations across multiple data views.

Contribution

It introduces a supervised deep generalized canonical correlation analysis method that considers multiple data views for nonlinear correlation modeling and phenotype discrimination.

Findings

Outperformed existing CCA-based and supervised methods in AD and cancer prediction.

Effectively identified biologically relevant multi-omics biomarkers.

Demonstrated capability for feature selection and gene clustering related to diseases.

Abstract

Integration of multi-omics data provides opportunities for revealing biological mechanisms related to certain phenotypes. We propose a novel method of multi-omics integration called supervised deep generalized canonical correlation analysis (SDGCCA) for modeling correlation structures between nonlinear multi-omics manifolds, aiming for improving classification of phenotypes and revealing biomarkers related to phenotypes. SDGCCA addresses the limitations of other canonical correlation analysis (CCA)-based models (e.g., deep CCA, deep generalized CCA) by considering complex/nonlinear cross-data correlations and discriminating phenotype groups. Although there are a few methods for nonlinear CCA projections for discriminant purposes of phenotypes, they only consider two views. On the other hand, SDGCCA is the nonlinear multiview CCA projection method for discrimination. When we applied SDGCCA to prediction of patients of Alzheimer's disease (AD) and discrimination of early- and late-stage cancers, it outperformed other CCA-based methods and other supervised methods. In addition, we demonstrate that SDGCCA can be used for feature selection to identify important multi-omics biomarkers. In the application on AD data, SDGCCA identified clusters of genes in multi-omics data, which are well known to be associated with AD.