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In this paper, we propose a methodology for deriving a model of a complex system by exploiting the information extracted from topological data analysis. Central to our approach is the S[B] paradigm in which a complex system is represented by a two-level model. One level, the structural S one, is derived using the newly-introduced quantitative concept of persistent entropy, and it is described by a persistent entropy automaton. The other level, the behavioral B one, is characterized by a network of interacting computational agents. The presented methodology is applied to a real case study, the idiotypic network of the mammalian immune system.

In the present work we intend to investigate how to detect the behaviour of the immune system reaction to an external stimulus in terms of phase transitions. The immune model considered follows Jerne’s idiotypic network theory. We considered two graph complexity measures—the connectivity entropy and the approximate von Neumann entropy—and one entropy for topological spaces, the so-called persistent entropy. The simplicial complex is obtained enriching the graph structure of the weighted idiotypic network, and it is formally analyzed by persistent homology and persistent entropy. We obtained numerical evidences that approximate von Neumann entropy and persistent entropy detect the activation of the immune system. In addition, persistent entropy allows also to identify the antibodies involved in the immune memory

Complex networks equipped with topological data analysis are one of the promising tools in the study of biological systems (e.g. evolution dynamics, brain correlation, breast cancer diagnosis, etc…). In this paper, we propose jHoles, a new version of Holes, an algorithms based on persistent homology for studying the connectivity features of complex networks. jHoles fills the lack of an efficient implementation of the filtering process for clique weight rank homology. We will give a brief overview of Holes, a more detailed description of jHoles algorithm, its implementation and the problem of clique weight rank homology. We present a biological case study showing how the connectivity of epidermal cells changes in response to a tumor presence. The biological network has been derived from the proliferative, differentiated and stratum corneum compartments, and jHoles used for studying variation of the connectivity