Luis M. Rocha @lmrocha@qoto.org

Author summary It is through social networks that contagious diseases spread in human populations, as best illustrated by the current pandemic and efforts to contain it. Measuring such networks from human contact data typically results in noisy and dense graphs that need to be simplified for effective analysis, without removal of their essential features. Thus, the identification of a primary subgraph that maintains the social interaction structure and likely transmission pathways is of relevance for studying epidemic spreading phenomena as well as devising intervention strategies to hinder spread. Here we propose and study the metric backbone as an optimal subgraph for sparsification of social contact networks in the study of simple spreading dynamics. We demonstrate that it is a unique, algebraically-principled network subgraph that preserves all shortest paths. We also discover that nine contact networks obtained from proximity sensors in a variety of social contexts contain large amounts of redundant interactions that can be removed with very little impact on community structure and epidemic spread. This reveals that epidemic spread on social networks is very robust to random interaction removal. However, extraction of the metric backbone subgraph reveals which interventions—strategic removal of specific social interactions—are likely to result in maximum impediment to epidemic spread.

New computational method developed by Instituto Gulbenkian de Ciência (IGC) scientists simplifies the analysis of social contacts.

Biomolecular network dynamics are thought to operate near the critical boundary between ordered and disordered regimes, where large perturbations to a small set of elements neither die out nor spread on average. A biomolecular automaton (e.g., gene, protein) typically has high regulatory redundancy, where small subsets of regulators determine activation via collective canalization. Previous work has shown that effective connectivity, a measure of collective canalization, leads to improved dynamical regime prediction for homogeneous automata networks. We expand this by (i) studying random Boolean networks (RBNs) with heterogeneous in-degree distributions, (ii) considering additional experimentally validated automata network models of biomolecular processes, and (iii) considering new measures of heterogeneity in automata network logic. We found that effective connectivity improves dynamical regime prediction in the models considered; in RBNs, combining effective connectivity with bias entropy further improves the prediction. Our work yields a new understanding of criticality in biomolecular networks that accounts for collective canalization, redundancy, and heterogeneity in the connectivity and logic of their automata models. The strong link we demonstrate between criticality and regulatory redundancy provides a means to modulate the dynamical regime of biochemical networks.

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Biomolecular network dynamics are thought to operate near the critical boundary between ordered and disordered regimes, where large perturbations to a small set of elements neither die out nor spread on average. A biomolecular automaton (e.g., gene, protein) typically has high regulatory redundancy, where small subsets of regulators determine activation via collective canalization. Previous work has shown that effective connectivity, a measure of collective canalization, leads to improved dynamical regime prediction for homogeneous automata networks. We expand this by (i) studying random Boolean networks (RBNs) with heterogeneous in-degree distributions, (ii) considering additional experimentally validated automata network models of biomolecular processes, and (iii) considering new measures of heterogeneity in automata network logic. We found that effective connectivity improves dynamical regime prediction in the models considered; in RBNs, combining effective connectivity with bias entropy further improves the prediction. Our work yields a new understanding of criticality in biomolecular networks that accounts for collective canalization, redundancy, and heterogeneity in the connectivity and logic of their automata models. The strong link we demonstrate between criticality and regulatory redundancy provides a means to modulate the dynamical regime of biochemical networks.

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AbstractMotivation. Cellular behavior is determined by complex non-linear interactions between numerous intracellular molecules that are often represented by Bo

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