Artículos de revistas
Learning Boolean logic models of signaling networks with ASP
Fecha
2015-09Registro en:
Videla, Santiago; Guziolowski, Carito; Eduati, Federica; Thiele, Sven; Gebser, Martin; et al.; Learning Boolean logic models of signaling networks with ASP; Elsevier Science; Theoretical Computer Science; 599; 9-2015; 79-101
0304-3975
Autor
Videla, Santiago
Guziolowski, Carito
Eduati, Federica
Thiele, Sven
Gebser, Martin
Nicolas, Jacques
Saez Rodriguez, Julio
Schaub, Torsten
Siegel, Anne
Resumen
Boolean networks provide a simple yet powerful qualitative modeling approach in systems biology. However, manual identification of logic rules underlying the system being studied is in most cases out of reach. Therefore, automated inference of Boolean logical networks from experimental data is a fundamental question in this field. This paper addresses the problem consisting of learning from a prior knowledge network describing causal interactions and phosphorylation activities at a pseudo-steady state, Boolean logic models of immediate-early response in signaling transduction networks. The underlying optimization problem has been so far addressed through mathematical programming approaches and the use of dedicated genetic algorithms. In a recent work we have shown severe limitations of stochastic approaches in this domain and proposed to use Answer Set Programming (ASP), considering a simpler problem setting. Herein, we extend our previous work in order to consider more realistic biological conditions including numerical datasets, the presence of feedback-loops in the prior knowledge networkand the necessity of multi-objective optimization. In order to cope with such extensions, we propose several discretization schemes and elaborate upon our previous ASP encoding. Towards real-world biological data, we evaluate the performance of our approach over in siliconumerical datasets based on a real and large-scale prior knowledge network. The correctness of our encoding and discretization schemes are dealt with in Appendices A–B.