Generalized simultaneous component analysis of binary and quantitative data

TL;DR

This paper introduces the generalized simultaneous component analysis (GSCA) model for integrating binary and quantitative data, addressing overfitting with a concave nuclear norm penalty, and demonstrates its effectiveness through simulations and real gene data analysis.

Contribution

The paper develops a novel GSCA model that combines binary and quantitative data analysis within a maximum likelihood framework, incorporating a concave penalty to prevent overfitting.

Findings

GSCA effectively recovers underlying data structures in simulations.

The model performs well with low signal-to-noise ratios.

Application to gene data demonstrates practical utility.

Abstract

In the current era of systems biological research there is a need for the integrative analysis of binary and quantitative genomics data sets measured on the same objects. One standard tool of exploring the underlying dependence structure present in multiple quantitative data sets is simultaneous component analysis (SCA) model. However, it does not have any provisions when a part of the data are binary. To this end, we propose the generalized SCA (GSCA) model, which takes into account the distinct mathematical properties of binary and quantitative measurements in the maximum likelihood framework. Like in the SCA model, a common low dimensional subspace is assumed to represent the shared information between these two distinct types of measurements. However, the GSCA model can easily be overfitted when a rank larger than one is used, leading to some of the estimated parameters to become very large. To achieve a low rank solution and combat overfitting, we propose to use a concave variant of the nuclear norm penalty. An efficient majorization algorithm is developed to fit this model with different concave penalties. Realistic simulations (low signal-to-noise ratio and highly imbalanced binary data) are used to evaluate the performance of the proposed model in recovering the underlying structure. Also, a missing value based cross validation procedure is implemented for model selection. We illustrate the usefulness of the GSCA model for exploratory data analysis of quantitative gene expression and binary copy number aberration (CNA) measurements obtained from the GDSC1000 data sets.