Efficient set-theoretic algorithms for computing high-order Forman-Ricci curvature on abstract simplicial complexes
Danillo Barros de Souza, Jonatas T. S. da Cunha, Fernando A. N. Santos, Jürgen Jost, Serafim Rodrigues
TL;DR
High-order Forman-Ricci curvature is powerful for capturing higher-order structure in networks but computationally expensive. The authors propose a set-theoretic formulation based on node neighbourhoods to enable efficient computation of $F_d(\alpha)$ for simplicial complexes, particularly Vietoris-Rips type where all simplices fill after the $1$-skeleton is present. They derive explicit expressions for neighborhoods ($N_\alpha$, $T_\alpha$, $P_\alpha$) and curvature, introduce FastForman with three variants, and demonstrate substantial improvements in time and memory compared to Hodgelaplacians and GeneralisedFormanRicci in benchmarks. This framework paves the way for scalable geometry-aware analysis in high-dimensional data and for extensions to cell complexes.
Abstract
Forman-Ricci curvature (FRC) is a potent and powerful tool for analysing empirical networks, as the distribution of the curvature values can identify structural information that is not readily detected by other geometrical methods. Crucially, FRC captures higher-order structural information of clique complexes of a graph or Vietoris-Rips complexes, which is not readily accessible to alternative methods. However, existing FRC platforms are prohibitively computationally expensive. Therefore, herein we develop an efficient set-theoretic formulation for computing such high-order FRC in simplicial complexes. Significantly, our set theory representation reveals previous computational bottlenecks and also accelerates the computation of FRC. Finally, We provide a pseudo-code, a software implementation coined FastForman, as well as a benchmark comparison with alternative implementations. We envisage that FastForman will be used in Topological and Geometrical Data analysis for high-dimensional complex data sets. Moreover, our development paves the way for future generalisations towards efficient computations of FRC on cell complexes.
