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David Šafránek

Publications and source records attributed to David Šafránek.

9 recordsLinked to original sources

Inference of Qualitative Models from Steady-State Data via Weighted MaxSMT

Qualitative models provide crucial instruments for modelling complex biological systems. While advances in automated reasoning and symbolic encodings have enabled rigorous inference of these models from data, the process remains highly fragile. First, biological measurement errors inevitably propagate into formal model specifications. Second, when a specification becomes unsatisfiable, distinguishing between fundamental design flaws and minor technical errors is notoriously difficult. This uncertainty often leads to under-specification, as it is unclear which observations are still ``safe'' to incorporate. To overcome these challenges, we introduce a robust inference method based on weighted MaxSMT. By encoding uncertain biological observations as weighted soft constraints, our approach enables the solver to identify a model best reflecting the observations, even with some conflicting constraints. Our method allows for Boolean and multi-valued variable domains, alongside observations derived from discretisation (level constraints) and differential expression (ordering constraints). We show our approach can be used to successfully infer neural cell differentiation models from prior-knowledge networks with 200--1300 genes using ordering constraints on all included genes.

q-bio.MN↗

BDD-Based Algorithm for SCC Decomposition of Edge-Coloured Graphs

Edge-coloured directed graphs provide an essential structure for modelling and analysis of complex systems arising in many scientific disciplines (e.g. feature-oriented systems, gene regulatory networks, etc.). One of the fundamental problems for edge-coloured graphs is the detection of strongly connected components, or SCCs. The size of edge-coloured graphs appearing in practice can be enormous both in the number of vertices and colours. The large number of vertices prevents us from analysing such graphs using explicit SCC detection algorithms, such as Tarjan's, which motivates the use of a symbolic approach. However, the large number of colours also renders existing symbolic SCC detection algorithms impractical. This paper proposes a novel algorithm that symbolically computes all the monochromatic strongly connected components of an edge-coloured graph. In the worst case, the algorithm performs $O(p \cdot n \cdot log~n)$ symbolic steps, where $p$ is the number of colours and $n$ is the number of vertices. We evaluate the algorithm using an experimental implementation based on binary decision diagrams (BDDs). Specifically, we use our implementation to explore the SCCs of a large collection of coloured graphs (up to $2^{48}$) obtained from Boolean networks -- a modelling framework commonly appearing in systems biology.

cs.DS↗

Robust Control of Partially Specified Boolean Networks

Regulatory networks (RNs) are a well-accepted modelling formalism in computational systems biology. The control of RNs is currently receiving a lot of attention because it provides a computational basis for cell reprogramming -- an attractive technology developed in regenerative medicine. By solving the control problem, we learn which parts of a biological system should be perturbed to stabilise the system in the desired phenotype. We allow the specification of the Boolean model representing a given RN to be incomplete. To that end, we utilise the formalism of partially specified Boolean networks which covers every possible behaviour of unspecified parts of the system. Such an approach causes a significant state explosion. This problem is addressed by using symbolic methods to represent both the unspecified model parts and all possible perturbations of the system. Additionally, to make the control design efficient and practically applicable, the optimal control should be minimal in terms of size. Moreover, in a partially specified model, a control may achieve the desired stabilisation only for a subset of the possible fully specified model instantiations. To address these aspects, we utilise several quantitative measures. Apart from the size of perturbation, we also examine its robustness -- a portion of instantiations for which the control is applicable. We show that proposed symbolic methods solving the control problem for partially specified BNs are efficient and scale well. We also evaluate the robustness metrics in cases of all three studied control types. The robustness metric tells us how big a proportion of fully defined systems the given perturbation works. Our experiments support the hypothesis that one-step perturbations may be less robust than temporary or permanent perturbations. This is a full version of a paper that is submitted to a journal.

eess.SY↗

Biochemical Space Language in Relation to Multiset Rewriting Systems

This technical report relates Biochemical Space Language (BCSL) to Multiset rewriting systems (MRS). For a BCSL model, the semantics are defined in terms of transition systems, while for an MRS, they are defined in terms of a set of runs. In this report, we relate BCSL to MRS by first showing how the transition system is related to a set of runs and consequently showing how for every BCSL model, an MRS can be constructed such that both represent the same set of runs. The motivation of this step is to establish BCSL in the context of a more general rewriting system and benefit from properties shown for them. Finally, we show that regulations defined for MRS can be consequently used in the BCSL model.

cs.LO↗

Regulated Multiset Rewriting Systems

Multiset rewriting systems provide a formalism particularly suitable for the description of biological systems. We present an extension of this formalism with additional controls on the derivations as a tool for reducing possible non-deterministic behaviour by providing additional knowledge about the system. We introduce several regulation mechanisms and compare their generative power.

cs.FL↗

Executable Biochemical Space for Specification and Analysis of Biochemical Systems

We present the second generation of a rule-based language called Biochemical Space Language (BCSL) that combines the advantages of different approaches and thus makes an effort to overcome several problems with existing solutions. The key aspect of the language is the level of abstraction it uses, which allows scalable and compact hierarchical specification of biochemical entities. This abstraction enables unique analysis techniques to reason about properties of models written in the language on the semantic and syntactic level.

q-bio.MN↗

Parameter Space Abstraction and Unfolding Semantics of Discrete Regulatory Networks

The modelling of discrete regulatory networks combines a graph specifying the pairwise influences between the variables of the system, and a parametrisation from which can be derived a discrete transition system. Given the influence graph only, the exploration of admissible parametrisations and the behaviours they enable is computationally demanding due to the combinatorial explosions of both parametrisation and reachable state space. This article introduces an abstraction of the parametrisation space and its refinement to account for the existence of given transitions, and for constraints on the sign and observability of influences. The abstraction uses a convex sublattice containing the concrete parametrisation space specified by its infimum and supremum parametrisations. It is shown that the computed abstractions are optimal, i.e., no smaller convex sublattice exists. Although the abstraction may introduce over-approximation, it has been proven to be conservative with respect to reachability of states. Then, an unfolding semantics for Parametric Regulatory Networks is defined, taking advantage of concurrency between transitions to provide a compact representation of reachable transitions. A prototype implementation is provided: it has been applied to several examples of Boolean and multi-valued networks, showing its tractability for networks with numerous components.

cs.DM↗

On Expressing and Monitoring Oscillatory Dynamics

To express temporal properties of dense-time real-valued signals, the Signal Temporal Logic (STL) has been defined by Maler et al. The work presented a monitoring algorithm deciding the satisfiability of STL formulae on finite discrete samples of continuous signals. The logic has been used to express and analyse biological systems, but it is not expressive enough to sufficiently distinguish oscillatory properties important in biology. In this paper we define the extended logic STL* in which STL is augmented with a signal-value freezing operator allowing us to express (and distinguish) detailed properties of biological oscillations. The logic is supported by a monitoring algorithm prototyped in Matlab. The monitoring procedure of STL* is evaluated on a biologically-relevant case study.

cs.CE↗

BioDiVinE: A Framework for Parallel Analysis of Biological Models

In this paper a novel tool BioDiVinEfor parallel analysis of biological models is presented. The tool allows analysis of biological models specified in terms of a set of chemical reactions. Chemical reactions are transformed into a system of multi-affine differential equations. BioDiVinE employs techniques for finite discrete abstraction of the continuous state space. At that level, parallel analysis algorithms based on model checking are provided. In the paper, the key tool features are described and their application is demonstrated by means of a case study.

cs.CE↗