Evidence map›Paper›PMID 39030497›Full record

ArticleBMC bioinformatics2024

TopoDoE: a design of experiment strategy for selection and refinement in ensembles of executable gene regulatory networks.

Matteo Bouvier, Souad Zreika, Elodie Vallin, Camille Fourneaux, Sandrine Gonin-Giraud, Arnaud Bonnaffoux, Olivier Gandrillon

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Article in BMC bioinformatics, 2024. 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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5 · Who and what money

Authors and funding

7 authors.

Matteo BouvierLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France. matteo.bouvier@ens-lyon.fr.
Souad ZreikaLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France.
Elodie VallinLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France.
Camille FourneauxLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France.
Sandrine Gonin-GiraudLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France.
Arnaud BonnaffouxVidium Solutions, Lyon, France.
Olivier GandrillonLaboratoire de Biologie Moléculaire de la Cellule, Lyon, France.

Funding

Agence Nationale de la Recherche ANR-17-CE12-0031
6 · The paper itself

Abstract

backgroundInference of Gene Regulatory Networks (GRNs) is a difficult and long-standing question in Systems Biology. Numerous approaches have been proposed with the latest methods exploring the richness of single-cell data. One of the current difficulties lies in the fact that many methods of GRN inference do not result in one proposed GRN but in a collection of plausible networks that need to be further refined. In this work, we present a Design of Experiment strategy to use as a second stage after the inference process. It is specifically fitted for identifying the next most informative experiment to perform for deciding between multiple network topologies, in the case where proposed GRNs are executable models. This strategy first performs a topological analysis to reduce the number of perturbations that need to be tested, then predicts the outcome of the retained perturbations by simulation of the GRNs and finally compares predictions with novel experimental data.

resultsWe apply this method to the results of our divide-and-conquer algorithm called WASABI, adapt its gene expression model to produce perturbations and compare our predictions with experimental results. We show that our networks were able to produce in silico predictions on the outcome of a gene knock-out, which were qualitatively validated for 48 out of 49 genes. Finally, we eliminate as many as two thirds of the candidate networks for which we could identify an incorrect topology, thus greatly improving the accuracy of our predictions.

conclusionThese results both confirm the inference accuracy of WASABI and show how executable gene expression models can be leveraged to further refine the topology of inferred GRNs. We hope this strategy will help systems biologists further explore their data and encourage the development of more executable GRN models.

Indexed as

AlgorithmsGene Regulatory NetworksComputational BiologyComputer SimulationModels, GeneticSystems BiologyDesign of experimentExecutable GRNGene regulatory network inferenceGRN ensembleGRN simulationPerturbation experiment

Identifiers

PMID39030497
PMCPMC11264509

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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.