Understanding diseases as increased heterogeneity: a complex network computational framework.

ABSTRACT: Owing to the complexity of the human body, most diseases present a high interpersonal variability in the way they manifest, i.e. in their phenotype, which has important clinical repercussions-for instance, the difficulty in defining objective diagnostic rules. Here we explore the hypothesis that signs and symptoms used to define a disease should be understood in terms of the dispersion (as opposed to the average) of physical observables. To that end, we propose a computational framework, based on complex networks theory, to map groups of subjects to a network structure, based on their pairwise phenotypical similarity. We demonstrate that the resulting structure can be used to improve the performance of classification algorithms, especially in the case of a limited number of instances, with

SUBMITTER: Zanin M 

PROVIDER: S-EPMC6127182 | biostudies-literature | 2018 Aug

REPOSITORIES: biostudies-literature