A generalized higher-order correlation analysis framework for multi-omics network inference

Multiple -omics (genomics, proteomics, etc.) profiles are commonly generated to gain insight into a disease or physiological system. Constructing multi-omics networks with respect to the trait(s) of interest provides an opportunity to understand relationships between molecular features but integration is challenging due to multiple data sets with high dimensionality. One approach is to use canonical correlation to integrate one or two omics types and a single trait of interest. However, these types of methods may be limited due to (1) not accounting for higher-order correlations existing among features, (2) computational inefficiency when extending to more than two omics data when using a penalty term-based sparsity method, and (3) lack of flexibility for focusing on specific correlations (e.g., omics-to-phenotype correlation versus omics-to-omics correlations). In this work, we have developed a novel multi-omics network analysis pipeline called Sparse Generalized Tensor Canonical Correlation Analysis Network Inference (SGTCCA-Net) that can effectively overcome these limitations. We also introduce an implementation to improve the summarization of networks for downstream analyses. Simulation and real-data experiments demonstrate the effectiveness of our novel method for inferring omics networks and features of interest.

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Publication Details

Journal
PLoS Computational Biology
Published
2025-04-14
DOI
https://doi.org/10.1371/journal.pcbi.1011842
Citations
3
Primary Topic
Bioinformatics and Genomic Networks
Type
article
Field-Weighted Citation Impact
2.42

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article

A generalized higher-order correlation analysis framework for multi-omics network inference

Farnoush Banaei‐Kashani, W. M. Liu, Russell Paul Bowler, Katherine Pratte et al.
3 citations
PLoS Computational Biology
Bioinformatics and Genomic Networks
2.42
article

A generalized higher-order correlation analysis framework for multi-omics network inference

Farnoush Banaei‐Kashani, W. M. Liu, Russell Paul Bowler, Katherine Pratte, Katerina Kechris, Craig P. Hersh, Peter J. Castaldi
article en
3 citations

Abstract

Multiple -omics (genomics, proteomics, etc.) profiles are commonly generated to gain insight into a disease or physiological system. Constructing multi-omics networks with respect to the trait(s) of interest provides an opportunity to understand relationships between molecular features but integration is challenging due to multiple data sets with high dimensionality. One approach is to use canonical correlation to integrate one or two omics types and a single trait of interest. However, these types of methods may be limited due to (1) not accounting for higher-order correlations existing among features, (2) computational inefficiency when extending to more than two omics data when using a penalty term-based sparsity method, and (3) lack of flexibility for focusing on specific correlations (e.g., omics-to-phenotype correlation versus omics-to-omics correlations). In this work, we have developed a novel multi-omics network analysis pipeline called Sparse Generalized Tensor Canonical Correlation Analysis Network Inference (SGTCCA-Net) that can effectively overcome these limitations. We also introduce an implementation to improve the summarization of networks for downstream analyses. Simulation and real-data experiments demonstrate the effectiveness of our novel method for inferring omics networks and features of interest.

PLoS Computational BiologyVol. 21(4)
Brigham and Women's Hospital (US), University of Denver (US), National Jewish Health (US), University of Colorado Anschutz Medical Campus (US), University of Colorado Denver (US)
National Institutes of Health, National Heart, Lung, and Blood Institute
Partnerships for the goals
Openalex Percentile: Top 12%
Bioinformatics and Genomic Networks
2.42
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