Trap spaces of Boolean networks are conflict-free siphons of their Petri net encoding.

Boolean network modeling of gene regulation but also of post-transcriptomic systems has proven over the years that it can bring powerful analyses and corresponding insight to the many cases where precise biological data is not sufficiently available to build a detailed quantitative model. Besides simulation, the analysis of such models is mostly based on attractor computation, since those correspond roughly to observable biological phenotypes. The recent use of trap spaces made a real breakthrough in that field allowing to consider medium-sized models that used to be out of reach. However, with the continuing increase in model size and complexity of Boolean update functions, the state-of-the-art computation of minimal trap spaces based on prime implicants shows its limits due to the difficulty of the prime-implicant computation.