Evidence map›Paper›PMID 40484997›Full record

ArticleBioinformatics (Oxford, England)2025

BiGSM: Bayesian inference of gene regulatory network via sparse modelling.

Hang Qin, Mateusz Garbulowski, Erik L L Sonnhammer, Saikat Chatterjee

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Hang QinDigital Futures, and School of Electrical Engineering and Computer Science, KTH Royal Institute of Technology, Stockholm 11428, Sweden.ORCID 0009-0009-0631-9382
Mateusz GarbulowskiDepartment of Biochemistry and Biophysics, Stockholm University, Science for Life Laboratory, Solna 17121, Sweden.ORCID 0000-0002-2497-194X
Erik L L SonnhammerDepartment of Biochemistry and Biophysics, Stockholm University, Science for Life Laboratory, Solna 17121, Sweden.ORCID 0000-0002-9015-5588
Saikat ChatterjeeDigital Futures, and School of Electrical Engineering and Computer Science, KTH Royal Institute of Technology, Stockholm 11428, Sweden.ORCID 0000-0003-2638-6047

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationInference of gene regulatory network (GRN) is challenging due to the inherent sparsity of the GRN matrix and noisy expression data, often leading to a high possibility of false positive or negative predictions. To address this, it is essential to leverage the sparsity of the GRN matrix and develop a robust method capable of handling varying levels of noise in the data. Moreover, most existing GRN inference methods produce only fixed point estimates, which lack the flexibility and informativeness for comprehensive network analysis. In contrast, a Bayesian approach that yields closed-form posterior distributions allows probabilistic link selection, offering insights into the statistical confidence of each possible link. Consequently, it is important to engineer a Bayesian GRN inference method and rigorously execute a benchmark evaluation compared to state-of-the-art methods.

resultsWe propose a method-Bayesian inference of GRN via Sparse Modelling (BiGSM). BiGSM effectively exploits the sparsity of the GRN matrix and infers the posterior distributions of GRN links from noisy expression data by using the maximum likelihood based learning. We thoroughly benchmarked BiGSM using biological and simulated datasets including GeneNetWeaver, GeneSPIDER, and GRNbenchmark. The benchmark test evaluates its accuracy and robustness across varying noise levels and data models. Using point-estimate based performance measures, BiGSM provides an overall best performance in comparison with several state-of-the-art methods including GENIE3, LASSO, LSCON, and Zscore. Additionally, BiGSM is the only method in the set of competing methods that provides posteriors for the GRN weights, helping to decipher confidence across predictions. AVAILABILITY AND IMPLEMENTATION: Code implemented via MATLAB and Python are available at Github: https://github.com/SachLab/BiGSM and archived at zenodo.

Indexed as

Computational BiologyGene Regulatory NetworksAlgorithmsBayes Theorem

Identifiers

PMID40484997
PMCPMC12151459

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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.