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KaSa: A Static Analyzer for Kappa

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Computational Methods in Systems Biology (CMSB 2018)

Abstract

KaSa is a static analyzer for Kappa models. Its goal is two-fold. Firstly, KaSa assists the modeler by warning about potential issues in the model. Secondly, KaSa may provide useful properties to check that what is implemented is what the modeler has in mind and to provide a quick overview of the model for the people who have not written it.

The cornerstone of KaSa is a fix-point engine which detects some patterns that may never occur whatever the evolution of the system may be. From this, many useful information may be collected: KaSa warns about rules that may never be applied, about potential irreversible transformations of proteins (that may not be reverted even thanks to an arbitrary number of computation steps) and about the potential formation of unbounded molecular compounds. Lastly, KaSa detects potential influences (activation/inhibition relation) between rules.

In this paper, we illustrate the main features of KaSa on a model of the extracellular activation of the transforming growth factor, TGF-b.

This material is based upon works partially sponsored by ANR (Chair of Excellence AbstractCell), the Defense Advanced Research Projects Agency (DARPA) and the U. S. Army Research Office under grant number W911NF-14-1-0367, and by the ITMO Plan Cancer 2014 (TGFSysBio project). The views, opinions, and/or findings contained in this article are those of the authors and should not be interpreted as representing the official views or policies, either expressed or implied, of ANR, DARPA, the U. S. Department of Defense, or ITMO.

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References

  1. Blinov, M., et al.: BioNetGen: software for rule-based modeling of signal transduction based on the interactions of molecular domains. Bioinformatics 20(17), 3289–3291 (2004)

    Article  Google Scholar 

  2. Fages, F., Soliman, S.: From reaction models to influence graphs and back: a theorem. In: Fisher, J. (ed.) FMSB 2008. LNCS, vol. 5054, pp. 90–102. Springer, Heidelberg (2008). https://doi.org/10.1007/978-3-540-68413-8_7

    Chapter  MATH  Google Scholar 

  3. Feret, J., Lý, K.: Reachability analysis via orthogonal sets of patterns. Electron. Notes Theor. Comput. Sci. 335, 27–48 (2018)

    Article  Google Scholar 

  4. Feret, J., Lý, K.: Local traces: an over-approximation of the behaviour of the proteins in rule-based models. IEEE/ACM TCBB (2018)

    Google Scholar 

  5. Gyori, B., et al.: From word models to executable models of signaling networks using automated assembly. bioRxiv (2017)

    Google Scholar 

  6. Horiguchi, M., Ota, M., Rifkin, D.: Matrix control of transforming growth factor-\(\beta \) function. J. Biochemistry 152(4), 321–329 (2012)

    Article  Google Scholar 

  7. Leroy, X., Doligez, D., Frisch, A., Garrigue, J., Rémy, D., Vouillon, J.: The OCaml system (2017). Release 4.06

    Google Scholar 

  8. Naldi, A., Berenguier, D., Fauré, A., Lopez, F., Thieffry, D., Chaouiya, C.: Logical modelling of regulatory networks with ginsim 2.3. Biosystems 97(2), 134–139 (2009)

    Article  Google Scholar 

  9. Suderman, R., Deeds, E.: Machines vs. ensembles: effective MAPK signaling through heterogeneous sets of protein complexes. PLoS Comput. Biol. 9(10), e1003278 (2013)

    Article  Google Scholar 

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Contribution

Jérôme Feret (2010-present) and Kim Quyên Lý (2015–2017) are the main contributors of KaSa. KaSa is integrated within the Kappa modeling platform whose main architect is Pierre Boutillier. In particular, Pierre Boutillier has integrated KaSa in the user interface of Kappa which may be used either online, or locally. The model of the extracellular activation of the transforming growth factor, TGF-b, has been assembled by Jean Coquet (2012–2017), Nathalie Théret (2012-present), Pierre Vignet (2016-present), and Ferdinanda Camporesi (2016-present). Jérôme Feret has written the paper.

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Correspondence to Jérôme Feret .

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Boutillier, P. et al. (2018). KaSa: A Static Analyzer for Kappa. In: Češka, M., Šafránek, D. (eds) Computational Methods in Systems Biology. CMSB 2018. Lecture Notes in Computer Science(), vol 11095. Springer, Cham. https://doi.org/10.1007/978-3-319-99429-1_17

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  • DOI: https://doi.org/10.1007/978-3-319-99429-1_17

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  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-319-99428-4

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