Bayesian Cox model with graph-structured variable selection priors for multi-omics biomarker identification

• URL: http://arxiv.org/abs/2503.13078v1
• Date: Mon, 17 Mar 2025 11:33:21 GMT
• Title: Bayesian Cox model with graph-structured variable selection priors for multi-omics biomarker identification
• Authors: Tobias Østmo Hermansen, Manuela Zucknick, Zhi Zhao,
• Abstract summary: We propose a penalized semiparametric Bayesian Cox model with graph-structured selection priors for sparse identification of multi-omics features.<n>We show that the proposed model results in more trustable and stable variable selection and non-inferior survival prediction.<n>The proposed model is applied to the primary invasive breast cancer patients data in The Cancer Genome Atlas project.
• Score: 0.0
• License: http://creativecommons.org/licenses/by/4.0/
• Abstract: An important goal in cancer research is the survival prognosis of a patient based on a minimal panel of genomic and molecular markers such as genes or proteins. Purely data-driven models without any biological knowledge can produce non-interpretable results. We propose a penalized semiparametric Bayesian Cox model with graph-structured selection priors for sparse identification of multi-omics features by making use of a biologically meaningful graph via a Markov random field (MRF) prior to capturing known relationships between multi-omics features. Since the fixed graph in the MRF prior is for the prior probability distribution, it is not a hard constraint to determine variable selection, so the proposed model can verify known information and has the potential to identify new and novel biomarkers for drawing new biological knowledge. Our simulation results show that the proposed Bayesian Cox model with graph-based prior knowledge results in more trustable and stable variable selection and non-inferior survival prediction, compared to methods modeling the covariates independently without any prior knowledge. The results also indicate that the performance of the proposed model is robust to a partially correct graph in the MRF prior, meaning that in a real setting where not all the true network information between covariates is known, the graph can still be useful. The proposed model is applied to the primary invasive breast cancer patients data in The Cancer Genome Atlas project.

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