Evidence map›Paper›PMID 36179082›Full record

ArticleBioinformatics (Oxford, England)2022

GeneNetTools: tests for Gaussian graphical models with shrinkage.

Victor Bernal, Venustiano Soancatl-Aguilar, Jonas Bulthuis, Victor Guryev, Peter Horvatovich, Marco Grzegorczyk

Abstract read
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Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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3 · Its place in the literature

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2 citing papers in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Victor BernalCenter of Information Technology, University of Groningen, Groningen 9747 AJ, The Netherlands.ORCID 0000-0002-9134-7186
Venustiano Soancatl-AguilarCenter of Information Technology, University of Groningen, Groningen 9747 AJ, The Netherlands.
Jonas BulthuisCenter of Information Technology, University of Groningen, Groningen 9747 AJ, The Netherlands.
Victor GuryevEuropean Research Institute for the Biology of Ageing, University Medical Center Groningen, University of Groningen, Groningen 9713 AV, The Netherlands.
Peter HorvatovichDepartment of Analytical Biochemistry, Groningen Research Institute of Pharmacy, University of Groningen, Groningen 9713 AV, The Netherlands.ORCID 0000-0003-2218-1140
Marco GrzegorczykDepartment of Mathematics, Bernoulli Institute, University of Groningen, Groningen 9747 AG, The Netherlands.

Funding

Center of Information TechnologyNWOUniversity of Groningen
6 · The paper itself

Abstract

motivationGaussian graphical models (GGMs) are network representations of random variables (as nodes) and their partial correlations (as edges). GGMs overcome the challenges of high-dimensional data analysis by using shrinkage methodologies. Therefore, they have become useful to reconstruct gene regulatory networks from gene-expression profiles. However, it is often ignored that the partial correlations are 'shrunk' and that they cannot be compared/assessed directly. Therefore, accurate (differential) network analyses need to account for the number of variables, the sample size, and also the shrinkage value, otherwise, the analysis and its biological interpretation would turn biased. To date, there are no appropriate methods to account for these factors and address these issues.

resultsWe derive the statistical properties of the partial correlation obtained with the Ledoit-Wolf shrinkage. Our result provides a toolbox for (differential) network analyses as (i) confidence intervals, (ii) a test for zero partial correlation (null-effects) and (iii) a test to compare partial correlations. Our novel (parametric) methods account for the number of variables, the sample size and the shrinkage values. Additionally, they are computationally fast, simple to implement and require only basic statistical knowledge. Our simulations show that the novel tests perform better than DiffNetFDR-a recently published alternative-in terms of the trade-off between true and false positives. The methods are demonstrated on synthetic data and two gene-expression datasets from Escherichia coli and Mus musculus. AVAILABILITY AND IMPLEMENTATION: The R package with the methods and the R script with the analysis are available in https://github.com/V-Bernal/GeneNetTools. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

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Gene Regulatory NetworksAnimalsGene ExpressionMiceNormal DistributionSample Size

Identifiers

PMID36179082
PMCPMC9665865

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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.