Abstract
Background Multi-omics integration may provide additional information about the development of tumors and improve the performance of predictive models. The key challenge lies in integrating several omics sources, especially to capture their biological relationships. Previous studies proposed a structural equation model framework to combine two data platforms for predicting survival; however, several limitations remain.
Results In this study, we introduce an extended Bayesian survival model combined with a structural equation model for adaptation to broader applications. The No U-turn Sampling (NUTS) algorithm was utilized to efficiently sample the posterior distribution of model parameters. Through a series of simulation studies, our model showed excellent goodness-of-fit and predictive performance. To validate the efficiency of our model, we utilized a gastric cancer dataset with three omics types (mRNA, microRNA, and methylation) obtained from The Cancer Genome Atlas. After bioinformatic processing, we included six mRNA, microRNA, and methylation loci datasets into the framework and discovered that our model exhibited greater predictive performance compared to non-integrated and Integrative Bayesian Analysis of Genomics (iBAG) models.
Conclusions In conclusion, our extended Bayesian structural equation model for multi-omics survival analysis provides a robust framework that significantly enhances predictive accuracy by effectively capturing complex biological relationships across diverse omics data sources, demonstrating clear advantages over both non-integrated approaches and existing integrative methods like iBAG.
© The Author(s) 2025.
Results In this study, we introduce an extended Bayesian survival model combined with a structural equation model for adaptation to broader applications. The No U-turn Sampling (NUTS) algorithm was utilized to efficiently sample the posterior distribution of model parameters. Through a series of simulation studies, our model showed excellent goodness-of-fit and predictive performance. To validate the efficiency of our model, we utilized a gastric cancer dataset with three omics types (mRNA, microRNA, and methylation) obtained from The Cancer Genome Atlas. After bioinformatic processing, we included six mRNA, microRNA, and methylation loci datasets into the framework and discovered that our model exhibited greater predictive performance compared to non-integrated and Integrative Bayesian Analysis of Genomics (iBAG) models.
Conclusions In conclusion, our extended Bayesian structural equation model for multi-omics survival analysis provides a robust framework that significantly enhances predictive accuracy by effectively capturing complex biological relationships across diverse omics data sources, demonstrating clear advantages over both non-integrated approaches and existing integrative methods like iBAG.
© The Author(s) 2025.
| Original language | English |
|---|---|
| Article number | 3 |
| Journal | BMC Bioinformatics |
| Volume | 27 |
| Issue number | 1 |
| Online published | 29 Nov 2025 |
| DOIs | |
| Publication status | Online published - 29 Nov 2025 |
Funding
This work was supported by the National Natural Science Foundation of China under Grant Number 81973143.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Research Keywords
- Bayesian framework
- Cancer
- Multi-omics
- Structural equation model
- Survival prediction
Publisher's Copyright Statement
- This full text is made available under CC-BY-NC-ND 4.0. https://creativecommons.org/licenses/by-nc-nd/4.0/
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