A latent factor model with a mixture of sparse and dense factors to model gene expression data with confounding effects

TL;DR

This paper introduces a Bayesian latent factor model with a mixture of sparse and dense factors to effectively analyze gene expression data, capturing both confounding effects and local gene interactions.

Contribution

It proposes a novel Bayesian model with layered shrinkage and a mixture component to distinguish between sparse and dense factors, automatically determining the number of factors.

Findings

Successfully recovered true latent structures in simulated data

Identified known covariates and gene groups in real data

Discovered biologically relevant genetic regulators

Abstract

One important problem in genome science is to determine sets of co-regulated genes based on measurements of gene expression levels across samples, where the quantification of expression levels includes substantial technical and biological noise. To address this problem, we developed a Bayesian sparse latent factor model that uses a three parameter beta prior to flexibly model shrinkage in the loading matrix. By applying three layers of shrinkage to the loading matrix (global, factor-specific, and element-wise), this model has non-parametric properties in that it estimates the appropriate number of factors from the data. We added a two-component mixture to model each factor loading as being generated from either a sparse or a dense mixture component; this allows dense factors that capture confounding noise, and sparse factors that capture local gene interactions. We developed two statistics to quantify the stability of the recovered matrices for both sparse and dense matrices. We tested our model on simulated data and found that we successfully recovered the true latent structure as compared to related models. We applied our model to a large gene expression study and found that we recovered known covariates and small groups of co-regulated genes. We validated these gene subsets by testing for associations between genotype data and these latent factors, and we found a substantial number of biologically important genetic regulators for the recovered gene subsets.