A knowledge representation meta-model for rule-based modelling of signalling networks

The study of cellular signalling pathways and their deregulation in disease states, such as cancer, is a large and extremely complex task. Indeed, these systems involve many parts and processes but are studied piecewise and their literatures and data are consequently fragmented, distributed and some...

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Main Authors: Adrien Basso-Blandin, Walter Fontana, Russ Harmer
Format: Article
Language:English
Published: Open Publishing Association 2016-03-01
Series:Electronic Proceedings in Theoretical Computer Science
Online Access:http://arxiv.org/pdf/1603.01488v1
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spelling doaj-627d2ac26b8344fc967837ee8080599c2020-11-25T01:08:49ZengOpen Publishing AssociationElectronic Proceedings in Theoretical Computer Science2075-21802016-03-01204Proc. DCM 2015475910.4204/EPTCS.204.5:2A knowledge representation meta-model for rule-based modelling of signalling networksAdrien Basso-Blandin0Walter Fontana1Russ Harmer2 LIP, ENS Lyon Harvard Medical School CNRS & LIP, ENS Lyon The study of cellular signalling pathways and their deregulation in disease states, such as cancer, is a large and extremely complex task. Indeed, these systems involve many parts and processes but are studied piecewise and their literatures and data are consequently fragmented, distributed and sometimes—at least apparently—inconsistent. This makes it extremely difficult to build significant explanatory models with the result that effects in these systems that are brought about by many interacting factors are poorly understood. The rule-based approach to modelling has shown some promise for the representation of the highly combinatorial systems typically found in signalling where many of the proteins are composed of multiple binding domains, capable of simultaneous interactions, and/or peptide motifs controlled by post-translational modifications. However, the rule-based approach requires highly detailed information about the precise conditions for each and every interaction which is rarely available from any one single source. Rather, these conditions must be painstakingly inferred and curated, by hand, from information contained in many papers—each of which contains only part of the story. In this paper, we introduce a graph-based meta-model, attuned to the representation of cellular signalling networks, which aims to ease this massive cognitive burden on the rule-based curation process. This meta-model is a generalization of that used by Kappa and BNGL which allows for the flexible representation of knowledge at various levels of granularity. In particular, it allows us to deal with information which has either too little, or too much, detail with respect to the strict rule-based meta-model. Our approach provides a basis for the gradual aggregation of fragmented biological knowledge extracted from the literature into an instance of the meta-model from which we can define an automated translation into executable Kappa programs.http://arxiv.org/pdf/1603.01488v1
collection DOAJ
language English
format Article
sources DOAJ
author Adrien Basso-Blandin
Walter Fontana
Russ Harmer
spellingShingle Adrien Basso-Blandin
Walter Fontana
Russ Harmer
A knowledge representation meta-model for rule-based modelling of signalling networks
Electronic Proceedings in Theoretical Computer Science
author_facet Adrien Basso-Blandin
Walter Fontana
Russ Harmer
author_sort Adrien Basso-Blandin
title A knowledge representation meta-model for rule-based modelling of signalling networks
title_short A knowledge representation meta-model for rule-based modelling of signalling networks
title_full A knowledge representation meta-model for rule-based modelling of signalling networks
title_fullStr A knowledge representation meta-model for rule-based modelling of signalling networks
title_full_unstemmed A knowledge representation meta-model for rule-based modelling of signalling networks
title_sort knowledge representation meta-model for rule-based modelling of signalling networks
publisher Open Publishing Association
series Electronic Proceedings in Theoretical Computer Science
issn 2075-2180
publishDate 2016-03-01
description The study of cellular signalling pathways and their deregulation in disease states, such as cancer, is a large and extremely complex task. Indeed, these systems involve many parts and processes but are studied piecewise and their literatures and data are consequently fragmented, distributed and sometimes—at least apparently—inconsistent. This makes it extremely difficult to build significant explanatory models with the result that effects in these systems that are brought about by many interacting factors are poorly understood. The rule-based approach to modelling has shown some promise for the representation of the highly combinatorial systems typically found in signalling where many of the proteins are composed of multiple binding domains, capable of simultaneous interactions, and/or peptide motifs controlled by post-translational modifications. However, the rule-based approach requires highly detailed information about the precise conditions for each and every interaction which is rarely available from any one single source. Rather, these conditions must be painstakingly inferred and curated, by hand, from information contained in many papers—each of which contains only part of the story. In this paper, we introduce a graph-based meta-model, attuned to the representation of cellular signalling networks, which aims to ease this massive cognitive burden on the rule-based curation process. This meta-model is a generalization of that used by Kappa and BNGL which allows for the flexible representation of knowledge at various levels of granularity. In particular, it allows us to deal with information which has either too little, or too much, detail with respect to the strict rule-based meta-model. Our approach provides a basis for the gradual aggregation of fragmented biological knowledge extracted from the literature into an instance of the meta-model from which we can define an automated translation into executable Kappa programs.
url http://arxiv.org/pdf/1603.01488v1
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