Threshold-free estimation of entropy from a Pearson matrix

There is demand in diverse fields for a reliable method of estimating the entropy associated with correlations. The estimation of a unique entropy directly from the Pearson correlation matrix has remained an open problem for more than half a century. All existing approaches lack generality insofar as they require thresholding choices that arbitrarily remove possibly important information. Here we propose an objective procedure for directly estimating a unique entropy of a general Pearson matrix. We show that upon rescaling the Pearson matrix satisfies all necessary conditions for an analog of the von Neumann entropy to be well defined. No thresholding is required. We demonstrate the method by estimating the entropy from neuroimaging time series of the human brain under the influence of a psychedelic

Neurological Diseases from a Systems Medicine Point of View.

The difficulty to understand, diagnose, and treat neurological disorders stems from the great complexity of the central nervous system on different levels of physiological granularity. The individual components, their interactions, and dynamics involved in brain development and function can be represented as molecular, cellular, or functional networks, where diseases are perturbations of networks. These networks can become a useful research tool in investigating neurological disorders if they are properly tailored to reflect corresponding mechanisms. Here, we review approaches to construct networks specific for neurological disorders describing disease-related pathology on different scales: the molecular, cellular, and brain level. We also briefly discuss cross-scale network analysis as a necessary integrator of these scales