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Discrete Bifurcation Analysis with Pithya

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14330%2F17%3A00114985" target="_blank" >RIV/00216224:14330/17:00114985 - isvavai.cz</a>

  • Výsledek na webu

  • DOI - Digital Object Identifier

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Discrete Bifurcation Analysis with Pithya

  • Popis výsledku v původním jazyce

    Bifurcation analysis is a central task of the analysis of parameterised high-dimensional dynamical systems that undergo transitions as parameters are changed. To characterise such transitions for models with many unknown parameters is a major challenge for complex, hence more realistic, models in systems biology. Its difficulty rises exponentially with the number of model components. The classical numerical and analytical methods for bifurcation analysis are typically limited to a small number of independent system parameters. To address this limitation we have developed a novel approach to bifurcation analysis called discrete bifurcation analysis, that is based on a suitable discrete abstraction of the given system and employs model checking for discovering critical parameter values, referred to as bifurcation points, for which various kinds of behaviour (equilibrium, cycling) appear or disappear. To describe such behaviour patterns, called phase portraits, we use a hybrid version of a CTL logic augmented with direction formulae. Technically, our approach is grounded in a novel method of parameter synthesis from temporal logic formulae using symbolic model checking and implemented in a new high-performance tool Pithya. Pithya itself implements state-of-the-art parameter synthesis methods. For a given ODE model, it allows to visually explore model behaviour with respect to different parameter values. Moreover, Pithya automatically synthesises parameter values satisfying a given property. Such property can specify various behaviour constraints, e.g., maximal reachable concentration, time ordering of events, characteristics of steady states, the presence of limit cycles, etc. The results can be visualised and explored in a graphical user interface. We demonstrate the method on a case study taken from biology describing the interaction of the tumour suppressor protein pRB and the central transcription factor E2F1. This system represents an important mechanism of a biological switch governing the transition from G1 to S phase in the mammalian cell cycle. In the G1-phase the cell makes an important decision. In high concentration levels, E2F1 activates the phase transition. In low concentration of E2F1, the transition to S-phase is rejected and the cell avoids division.

  • Název v anglickém jazyce

    Discrete Bifurcation Analysis with Pithya

  • Popis výsledku anglicky

    Bifurcation analysis is a central task of the analysis of parameterised high-dimensional dynamical systems that undergo transitions as parameters are changed. To characterise such transitions for models with many unknown parameters is a major challenge for complex, hence more realistic, models in systems biology. Its difficulty rises exponentially with the number of model components. The classical numerical and analytical methods for bifurcation analysis are typically limited to a small number of independent system parameters. To address this limitation we have developed a novel approach to bifurcation analysis called discrete bifurcation analysis, that is based on a suitable discrete abstraction of the given system and employs model checking for discovering critical parameter values, referred to as bifurcation points, for which various kinds of behaviour (equilibrium, cycling) appear or disappear. To describe such behaviour patterns, called phase portraits, we use a hybrid version of a CTL logic augmented with direction formulae. Technically, our approach is grounded in a novel method of parameter synthesis from temporal logic formulae using symbolic model checking and implemented in a new high-performance tool Pithya. Pithya itself implements state-of-the-art parameter synthesis methods. For a given ODE model, it allows to visually explore model behaviour with respect to different parameter values. Moreover, Pithya automatically synthesises parameter values satisfying a given property. Such property can specify various behaviour constraints, e.g., maximal reachable concentration, time ordering of events, characteristics of steady states, the presence of limit cycles, etc. The results can be visualised and explored in a graphical user interface. We demonstrate the method on a case study taken from biology describing the interaction of the tumour suppressor protein pRB and the central transcription factor E2F1. This system represents an important mechanism of a biological switch governing the transition from G1 to S phase in the mammalian cell cycle. In the G1-phase the cell makes an important decision. In high concentration levels, E2F1 activates the phase transition. In low concentration of E2F1, the transition to S-phase is rejected and the cell avoids division.

Klasifikace

  • Druh

    D - Stať ve sborníku

  • CEP obor

  • OECD FORD obor

    10201 - Computer sciences, information science, bioinformathics (hardware development to be 2.2, social aspect to be 5.8)

Návaznosti výsledku

  • Projekt

    Výsledek vznikl pri realizaci vícero projektů. Více informací v záložce Projekty.

  • Návaznosti

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)<br>S - Specificky vyzkum na vysokych skolach

Ostatní

  • Rok uplatnění

    2017

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název statě ve sborníku

    15th International Conference on Computational Methods in Systems Biology (CMSB)

  • ISBN

    9783319674704

  • ISSN

    0302-9743

  • e-ISSN

  • Počet stran výsledku

    2

  • Strana od-do

    319-320

  • Název nakladatele

    Springer

  • Místo vydání

    Cham

  • Místo konání akce

    Darmstadt

  • Datum konání akce

    27. 9. 2017

  • Typ akce podle státní příslušnosti

    WRD - Celosvětová akce

  • Kód UT WoS článku

    000542715600021