701 research outputs found

    Brane Calculi Systems: A Static Preview of their Possible Behaviour

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    We improve the precision of a previous Control Flow Analysis for Brane Calculi, by adding information on the context and introducing causality information on the membranes. This allows us to prove some biological properties on the behaviour of systems specified in Brane Calculi.Comment: Presented at MeCBIC 201

    Process Calculi Abstractions for Biology

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    Several approaches have been proposed to model biological systems by means of the formal techniques and tools available in computer science. To mention just a few of them, some representations are inspired by Petri Nets theory, and some other by stochastic processes. A most recent approach consists in interpreting the living entities as terms of process calculi where the behavior of the represented systems can be inferred by applying syntax-driven rules. A comprehensive picture of the state of the art of the process calculi approach to biological modeling is still missing. This paper goes in the direction of providing such a picture by presenting a comparative survey of the process calculi that have been used and proposed to describe the behavior of living entities. This is the preliminary version of a paper that was published in Algorithmic Bioprocesses. The original publication is available at http://www.springer.com/computer/foundations/book/978-3-540-88868-

    Drip and Mate Operations Acting in Test Tube Systems and Tissue-like P systems

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    The operations drip and mate considered in (mem)brane computing resemble the operations cut and recombination well known from DNA computing. We here consider sets of vesicles with multisets of objects on their outside membrane interacting by drip and mate in two different setups: in test tube systems, the vesicles may pass from one tube to another one provided they fulfill specific constraints; in tissue-like P systems, the vesicles are immediately passed to specified cells after having undergone a drip or mate operation. In both variants, computational completeness can be obtained, yet with different constraints for the drip and mate operations

    Finite group discretization of Yang-Mills and Einstein actions

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    Discrete versions of the Yang-Mills and Einstein actions are proposed for any finite group. These actions are invariant respectively under local gauge transformations, and under the analogues of Lorentz and general coordinate transformations. The case Z_n \times Z_n \times...\times Z_n is treated in some detail, recovering the Wilson action for Yang-Mills theories, and a new discretized action for gravity.Comment: LaTeX file, 23 page

    Modelling Cell Cycle using Different Levels of Representation

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    Understanding the behaviour of biological systems requires a complex setting of in vitro and in vivo experiments, which attracts high costs in terms of time and resources. The use of mathematical models allows researchers to perform computerised simulations of biological systems, which are called in silico experiments, to attain important insights and predictions about the system behaviour with a considerably lower cost. Computer visualisation is an important part of this approach, since it provides a realistic representation of the system behaviour. We define a formal methodology to model biological systems using different levels of representation: a purely formal representation, which we call molecular level, models the biochemical dynamics of the system; visualisation-oriented representations, which we call visual levels, provide views of the biological system at a higher level of organisation and are equipped with the necessary spatial information to generate the appropriate visualisation. We choose Spatial CLS, a formal language belonging to the class of Calculi of Looping Sequences, as the formalism for modelling all representation levels. We illustrate our approach using the budding yeast cell cycle as a case study

    Noncommutative Geometry and D-Branes

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    We apply noncommutative geometry to a system of N parallel D-branes, which is interpreted as a quantum space. The Dirac operator defining the quantum differential calculus is identified to be the supercharge for strings connecting D-branes. As a result of the calculus, Connes' Yang-Mills action functional on the quantum space reproduces the dimensionally reduced U(N) super Yang-Mills action as the low energy effective action for D-brane dynamics. Several features that may look ad hoc in a noncommutative geometric construction are shown to have very natural physical or geometric origin in the D-brane picture in superstring theory.Comment: 16 pages, Latex, typos corrected and minor modification mad

    Measurable Stochastics for Brane Calculus

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    We give a stochastic extension of the Brane Calculus, along the lines of recent work by Cardelli and Mardare. In this presentation, the semantics of a Brane process is a measure of the stochastic distribution of possible derivations. To this end, we first introduce a labelled transition system for Brane Calculus, proving its adequacy w.r.t. the usual reduction semantics. Then, brane systems are presented as Markov processes over the measurable space generated by terms up-to syntactic congruence, and where the measures are indexed by the actions of this new LTS. Finally, we provide a SOS presentation of this stochastic semantics, which is compositional and syntax-driven.Comment: In Proceedings MeCBIC 2010, arXiv:1011.005

    Formal executable descriptions of biological systems

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    The similarities between systems of living entities and systems of concurrent processes may support biological experiments in silico. Process calculi offer a formal framework to describe biological systems, as well as to analyse their behaviour, both from a qualitative and a quantitative point of view. A couple of little examples help us in showing how this can be done. We mainly focus our attention on the qualitative and quantitative aspects of the considered biological systems, and briefly illustrate which kinds of analysis are possible. We use a known stochastic calculus for the first example. We then present some statistics collected by repeatedly running the specification, that turn out to agree with those obtained by experiments in vivo. Our second example motivates a richer calculus. Its stochastic extension requires a non trivial machinery to faithfully reflect the real dynamic behaviour of biological systems
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