Evidence map›Paper›PMID 41166379›Full record

ArticlePLoS computational biology2025

HMFGraph: Novel Bayesian approach for recovering biological networks.

Aapo E Korhonen, Olli Sarala, Tuomas Hautamäki, Markku Kuismin, Mikko J Sillanpää

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Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Aapo E KorhonenResearch Unit of Mathematical Sciences, University of Oulu, Oulu, Finland.ORCID 0009-0007-6156-3121
Olli SaralaResearch Unit of Mathematical Sciences, University of Oulu, Oulu, Finland.
Tuomas HautamäkiResearch Unit of Mathematical Sciences, University of Oulu, Oulu, Finland.ORCID 0009-0004-4641-3828
Markku KuisminResearch Unit of Mathematical Sciences, University of Oulu, Oulu, Finland.
Mikko J SillanpääResearch Unit of Mathematical Sciences, University of Oulu, Oulu, Finland.ORCID 0000-0003-2808-2768

Funding

Finnish Doctoral Program Network in Artificial Intelligence, AI-DOCResearch Council of FinlandYrjö and Kalle Väisälä Foundation
6 · The paper itself

Abstract

Gaussian graphical models (GGM) are powerful tools to examine partial correlation structures in high-dimensional omics datasets. Partial correlation networks can explain complex relationships between genes or other biological variables. Bayesian implementations of GGMs have recently received more attention. Usually, the most demanding parts of GGM implementations are: (i) hyperparameter tuning, (ii) edge selection, (iii) scalability for large datasets, and (iv) the prior choice for Bayesian GGM. To address these limitations, we introduce a novel Bayesian GGM using a hierarchical matrix-F prior with a fast implementation. We show, with extensive simulations and biological example analyses, that this prior has competitive network recovery capabilities compared to state-of-the-art approaches and good properties for recovering meaningful networks. We present a new way of tuning the shrinkage hyperparameter by constraining the condition number of the estimated precision matrix. For edge selection, we propose using approximated credible intervals (CI) whose width is controlled by the false discovery rate. An optimal CI is selected by maximizing an estimated F1-score via permutations. In addition, a specific choice of hyperparameter can make the proposed prior better suited for clustering and community detection. Our method, with a generalized expectation-maximization algorithm, computationally outperforms existing Bayesian GGM approaches that use Markov chain Monte Carlo algorithms. The method is implemented in the R package HMFGraph, found on GitHub at https://github.com/AapoKorhonen/HMFGraph. All codes to reproduce the results are found on GitHub at https://github.com/AapoKorhonen/HMFGraph-Supplementary.

Indexed as

Computational BiologyGene Regulatory NetworksAlgorithmsBayes TheoremComputer SimulationHumansNormal DistributionSoftware

Identifiers

PMID41166379
PMCPMC12591435

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.