Parallel One-Step Control of Parametrised Boolean Networks

TL;DR

This paper introduces a semi-symbolic algorithm for controlling parametrised Boolean networks efficiently, avoiding exhaustive parameter scanning, and demonstrates its effectiveness on biological models.

Contribution

It presents the first control method for ParBNs with asynchronous semantics using a semi-symbolic approach, improving efficiency over naive parameter scan methods.

Findings

The proposed algorithm outperforms naive methods on biological models.

It effectively stabilizes systems with minimal interventions.

The approach handles the exponential parameter space efficiently.

Abstract

Boolean network (BN) is a simple model widely used to study complex dynamic behaviour of biological systems. Nonetheless, it might be difficult to gather enough data to precisely capture the behavior of a biological system into a set of Boolean functions. These issues can be dealt with to some extent using parametrised Boolean networks (ParBNs), as it allows to leave some update functions unspecified. In this paper, we attack the control problem for ParBNs with asynchronous semantics. While there is an extensive work on controlling BNs without parameters, the problem of control for ParBNs has not been in fact addressed yet. The goal of control is to ensure the stabilisation of a system in a given state using as few interventions as possible. There are many ways to control BN dynamics. Here, we consider the one-step approach in which the system is instantaneously perturbed out of its actual state. A naive approach to handle control of ParBNs is using parameter scan and solve the control problem for each parameter valuation separately using known techniques for non-parametrised BNs. This approach is however highly inefficient as the parameter space of ParBNs grows doubly-exponentially in the worst case. In this paper, we propose a novel semi-symbolic algorithm for the one-step control problem of ParBNs, that builds on a symbolic data structures to avoid scanning individual parameters. We evaluate the performance of our approach on real biological models.