Uncovering Multi-Omics Profiles of Population Heterogeneity: A Cluster-Based Bayesian Approach
Runye ShiiD, Ziyang Xiong, Tobias BanaschewskiiD, Gareth J. BarkeriD, Arun L.W. BokdeiD, Herta FloriD, Hugh GaravaniD, Penny Anne GowlandiD, Antoine GrigisiD, Andreas HeinziD, Jean‐Luc MartinotiD, Marie‐Laure Paillère MartinotiD, Eric Artiges AiD, Frauke NeesiD, Dimitri Papadopoulos OrfanosiD, Luise PoustkaiD, Michael N. SmolkaiD, Sarah HohmanniD, Nilakshi VaidyaiD, Henrik WalteriD, Robert WhelaniD, Günter SchumanniD, Sylvane DesrivièresiD, Xiaolei LiniD, Jianfeng Feng
Abstract
Understanding the heterogeneous nature of genetic effects is critical for advancing our knowledge of the genetic architecture of complex traits and developing personalized management strategies. However, existing methods often rely on pre-specified modifying variables to model this heterogeneity, limiting their ability to capture effects driven by complex or unobserved factors. Here, we propose MOCHA (Multi-Omics Clustering for Heterogeneous Association), a novel Bayesian analytical paradigm that identifies latent population subgroups with distinct genetic effects directly from multi-omics data, without requiring a priori variable specification. Extensive simulations confirm that MOCHA accurately identifies the underlying clustering structure, demonstrates superior performance in identifying and ranking features with cluster-specific effects, and provides reliable parameter estimates. Applying MOCHA to genomic and transcriptomic data from the IMAGEN study, we identified two distinct neurodevelopmental clusters associated with adolescent inhibitory control. Post-hoc characterization of these clusters provided novel insights into the mechanisms of brain plasticity, demonstrating the methods practical utility and interpretability.
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