General Kernel Machine Methods for Multi-Omics Integration and Genome-Wide Association Testing With Related Individuals

Amarise Little*, Ni Zhao, Anna Mikhaylova, Angela Zhang, Wodan Ling, Florian Thibord, Andrew D Johnson, Laura M Raffield, Joanne E Curran, John Blangero, Jeffrey R O'Connell, Huichun Xu, Jerome I Rotter, Stephen S Rich, Kenneth M Rice, Ming-Huei Chen, Alexander Reiner, Charles Kooperberg, Thao Vu, Lifang HouMyriam Fornage, Ruth J F Loos, Eimear Kenny, Rasika Mathias, Lewis Becker, Albert V Smith, Eric Boerwinkle, Bing Yu, Timothy Thornton, Michael C Wu

*Corresponding author for this work

Research output: Contribution to journalJournal articleResearchpeer-review

Abstract

Integrating multi-omics data may help researchers understand the genetic underpinnings of complex traits and diseases. However, the best ways to integrate multi-omics data and use them to address pressing scientific questions remain a challenge. One important and topical problem is how to assess the aggregate effect of multiple genomic data types (e.g. genotypes and gene expression levels) on a phenotype, particularly while accommodating routine issues, such as having related subjects' data in analyses. In this paper, we extend an existing composite kernel machine regression model to integrate two multi-omics data types, while accommodating for general correlation structures amongst outcomes. Due to the kernel machine regression framework, our methods allow for the integration of high-dimensional omics data with small, nonlinear, and interactive effects, and accommodation of general study designs. Here, we focus on scientific questions that aim to assess the association between a functional grouping (such as a gene or a pathway) and a quantitative trait of interest. We use a kernel machine regression to integrate the two multi-omics data types, as they may relate to the trait, and perform a global test of association. We demonstrate the advantage of this approach over single data type association tests via simulation. Finally, we apply this method to a large, multi-ethnic data set to investigate how predicted gene expression and rare genetic variation may be related to two platelet traits.

Original languageEnglish
Article numbere22610
JournalGenetic Epidemiology
Volume49
Issue number1
Number of pages17
ISSN0741-0395
DOIs
Publication statusPublished - 2025

Bibliographical note

© 2025 Wiley Periodicals LLC.

Keywords

  • Humans
  • Genome-Wide Association Study/methods
  • Genomics/methods
  • Phenotype
  • Algorithms
  • Models, Genetic
  • Polymorphism, Single Nucleotide
  • Genotype
  • Computer Simulation
  • Machine Learning
  • Multiomics

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