Evidence map›Paper›PMID 23079107›Full record

ArticleBMC systems biology2012

CellNOptR: a flexible toolkit to train protein signaling networks to data using multiple logic formalisms.

Camille Terfve, Thomas Cokelaer, David Henriques, Aidan MacNamara, Emanuel Goncalves, Melody K Morris, Martijn van Iersel, Douglas A Lauffenburger, Julio Saez-Rodriguez

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Article in BMC systems biology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

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108citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

108 citing papers in PubMed.

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  8. Automated model refinement using perturbation-observation pairs.NPJ systems biology and applications · 2025
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48 more citing papers are in PubMed but not listed here.

4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Camille TerfveEuropean Bioinformatics Institute, Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK.
Thomas Cokelaer
David Henriques
Aidan MacNamara
Emanuel Goncalves
Melody K Morris
Martijn van Iersel
Douglas A Lauffenburger
Julio Saez-Rodriguez

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCells process signals using complex and dynamic networks. Studying how this is performed in a context and cell type specific way is essential to understand signaling both in physiological and diseased situations. Context-specific medium/high throughput proteomic data measured upon perturbation is now relatively easy to obtain but formalisms that can take advantage of these features to build models of signaling are still comparatively scarce.

resultsHere we present CellNOptR, an open-source R software package for building predictive logic models of signaling networks by training networks derived from prior knowledge to signaling (typically phosphoproteomic) data. CellNOptR features different logic formalisms, from Boolean models to differential equations, in a common framework. These different logic model representations accommodate state and time values with increasing levels of detail. We provide in addition an interface via Cytoscape (CytoCopteR) to facilitate use and integration with Cytoscape network-based capabilities.

conclusionsModels generated with this pipeline have two key features. First, they are constrained by prior knowledge about the network but trained to data. They are therefore context and cell line specific, which results in enhanced predictive and mechanistic insights. Second, they can be built using different logic formalisms depending on the richness of the available data. Models built with CellNOptR are useful tools to understand how signals are processed by cells and how this is altered in disease. They can be used to predict the effect of perturbations (individual or in combinations), and potentially to engineer therapies that have differential effects/side effects depending on the cell type or context.

Indexed as

Data Interpretation, StatisticalLogicSignal TransductionSoftwareComputational BiologyHep G2 CellsHumansLiver NeoplasmsModels, BiologicalProteinsUser-Computer InterfaceProteins

Identifiers

PMID23079107
PMCPMC3605281

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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.