SCALABLE MULTIPLE NETWORK INFERENCE WITH THE JOINT GRAPHICAL HORSESHOE

• 成果类型: Article
• 署名作者: Lingjaerde, Camilla; Fairfax, Benjamin P.; Richardson, Sylvia; Ruffieux, Helene
• 署名单位: MRC Biostatistics Unit; University of Cambridge; University of Oxford
• 刊物名称: ANNALS OF APPLIED STATISTICS
• ISSN/ISSBN: 1932-6157
• DOI: 10.1214/23-AOAS1863
• 发表日期: 2024
• 页码: 1899-1923
• 关键词: inverse covariance estimation; maximum-likelihood; variable-selection; gene-expression; Lasso; estimator; aire; arylformamidase; hotspots

摘要

Network models are useful tools for modelling complex associations. In statistical omics such models are increasingly popular for identifying and assessing functional relationships and pathways. If a Gaussian graphical model is assumed, conditional independence is determined by the nonzero entries of the inverse covariance (precision) matrix of the data. The Bayesian graphical horseshoe estimator provides a robust and flexible framework for precision matrix inference, as it introduces local, edge-specific parameters which prevent over-shrinkage of nonzero off-diagonal elements. However, its applicability is currently limited in statistical omics settings, which often involve high-dimensional data from multiple conditions that might share common structures. We propose: (i) a scalable expectation conditional maximisation (ECM) algorithm for the original graphical horseshoe and (ii) a novel joint graphical horseshoe estimator, which borrows information across multiple related networks to improve estimation. We show numerically that our single-network ECM approach is more scalable than the existing graphical horseshoe Gibbs implementation, while achieving the same level of accuracy. We also show that our joint-network proposal successfully leverages shared edge-specific information between networks while still retaining differences, outperforming state-of-the-art methods at any level of network similarity. Finally, we leverage our approach to clarify gene regulation activity within and across immune stimulation conditions in monocytes, and formulate hypotheses on the pathogenesis of immune-mediated diseases.