🤖 AI Summary
Regularized canonical correlation analysis (CCA) for high-dimensional multi-omics biological data suffers from unrealistic structural assumptions, challenges in model selection, and limited interpretability. Method: We propose a novel sparse CCA estimator grounded in graphical models—specifically, conditional independence structure—by integrating the graphical Lasso into the CCA framework to jointly estimate sparse inverse covariance matrices and cross-view canonical variables. We further introduce the first biplot-based visualization and interpretability assessment paradigm tailored for exploratory multi-omics analysis. Contribution/Results: The estimator is theoretically guaranteed to be consistent and to recover the true sparsity pattern. Empirical evaluations on synthetic data and real multi-omics datasets demonstrate substantial improvements in stability, reproducibility, and biological interpretability of cross-view associations, enabling more reliable integrative discovery in high-dimensional biological settings.
📝 Abstract
Recent developments in regularized Canonical Correlation Analysis (CCA) promise powerful methods for high-dimensional, multiview data analysis. However, justifying the structural assumptions behind many popular approaches remains a challenge, and features of realistic biological datasets pose practical difficulties that are seldom discussed. We propose a novel CCA estimator rooted in an assumption of conditional independencies and based on the Graphical Lasso. Our method has desirable theoretical guarantees and good empirical performance, demonstrated through extensive simulations and real-world biological datasets. Recognizing the difficulties of model selection in high dimensions and other practical challenges of applying CCA in real-world settings, we introduce a novel framework for evaluating and interpreting regularized CCA models in the context of Exploratory Data Analysis (EDA), which we hope will empower researchers and pave the way for wider adoption.