Evidence map›Paper›PMID 27716031›Full record

ArticleBMC bioinformatics2016

Boolean regulatory network reconstruction using literature based knowledge with a genetic algorithm optimization method.

Julien Dorier, Isaac Crespo, Anne Niknejad, Robin Liechti, Martin Ebeling, Ioannis Xenarios

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed.

  1. Automated model refinement using perturbation-observation pairs.NPJ systems biology and applications · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Julien DorierVital-IT, Systems biology and medicine department, SIB Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland. julien.dorier@sib.swiss.ORCID http://orcid.org/0000-0002-6717-2451
Isaac CrespoVital-IT, Systems biology and medicine department, SIB Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland.
Anne NiknejadVital-IT, Systems biology and medicine department, SIB Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland.
Robin LiechtiVital-IT, Systems biology and medicine department, SIB Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland.
Martin EbelingPharmaceutical Sciences/Translational Technologies and Bioinformatics, Roche Innovation Center Basel, 124 Grenzacherstrasse, 4070, Basel, Switzerland.
Ioannis XenariosVital-IT, Systems biology and medicine department, SIB Swiss Institute of Bioinformatics, 1015, Lausanne, Switzerland. ioannis.xenarios@sib.swiss.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrior knowledge networks (PKNs) provide a framework for the development of computational biological models, including Boolean models of regulatory networks which are the focus of this work. PKNs are created by a painstaking process of literature curation, and generally describe all relevant regulatory interactions identified using a variety of experimental conditions and systems, such as specific cell types or tissues. Certain of these regulatory interactions may not occur in all biological contexts of interest, and their presence may dramatically change the dynamical behaviour of the resulting computational model, hindering the elucidation of the underlying mechanisms and reducing the usefulness of model predictions. Methods are therefore required to generate optimized contextual network models from generic PKNs.

resultsWe developed a new approach to generate and optimize Boolean networks, based on a given PKN. Using a genetic algorithm, a model network is built as a sub-network of the PKN and trained against experimental data to reproduce the experimentally observed behaviour in terms of attractors and the transitions that occur between them under specific perturbations. The resulting model network is therefore contextualized to the experimental conditions and constitutes a dynamical Boolean model closer to the observed biological process used to train the model than the original PKN. Such a model can then be interrogated to simulate response under perturbation, to detect stable states and their properties, to get insights into the underlying mechanisms and to generate new testable hypotheses.

conclusionsGeneric PKNs attempt to synthesize knowledge of all interactions occurring in a biological process of interest, irrespective of the specific biological context. This limits their usefulness as a basis for the development of context-specific, predictive dynamical Boolean models. The optimization method presented in this article produces specific, contextualized models from generic PKNs. These contextualized models have improved utility for hypothesis generation and experimental design. The general applicability of this methodological approach makes it suitable for a variety of biological systems and of general interest for biological and medical research. Our method was implemented in the software optimusqual, available online at http://www.vital-it.ch/software/optimusqual/ .

Indexed as

AlgorithmsComputer SimulationGene Regulatory NetworksKnowledge BasesModels, GeneticHumansModels, BiologicalPublicationsSoftwareBoolean regulatory networksGenetic algorithmNetwork inferenceOptimizationPrior knowledge networkQualitative modeling

Identifiers

PMID27716031
PMCPMC5053080

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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.