Bayesian Computational Neuroscience

In this Section:

Example fMRI image, overlaid with partial DBN analysis results Schizophrenia is an illness with enormous public health significance, affecting over 30 million people and inflicting immense personal and economic cost worldwide. Treatments for this terrible disease are still limited, at least in part because of poor understanding its anatomical, neural, cognitive, and genetic substrates. Modern morphometric and functional neuroimaging technologies can provide us noninvasive views of the behavior of the schizophrenic brain, but identifying significant circuits (and, worse, misconnections or breakdowns in circuits) in such rich data sources is a challenging problem.

Example DBN structural model In this work, my research group and our colleagues at The MIND Research Network are developing advanced dynamic Bayesian network (DBN) analysis methods to infer and model functional activity networks from neuroimaging data. Given functional neuroimaging data (fMRI, MEG, and/or EEG) gathered from both healthy and schizophrenic patients, we attempt to find DBNs that characterize each of the populations and/or the differences between the populations. The conditional independence relations encoded in these models provide semantic indications of brain activity networks. The content of the conditional probability tables descibe the form of the functional relationships among related regions.


This approach provides three distinct approaches over existing modeling mechanisms for functional neuroimaging data:

Data driven
By employing Bayesian Network structure search mechanisms, we can identify independence relations directly via their posterior probabilities. Thus, our methods do not require strong initial anatomical connectivity or hypothesis-driven model assumptions.
Nonlinear
Unlike common linear Gaussian dynamical models, we take our conditional probability distribution family to be discrete multinomials. Multinomials are a universal function familiy over the finite-dimensional simplex, so we have the capacity to represent any, arbitrarily nonlinear functional relationship among random variables.
Multivariate
DBNs capture the statistical dependence relationships among sets of variables. Thus, rather than characterising the relationship of only pairs of regions or of all regions simultaneously (e.g., under a linear combination model), we can identify small, discrete groups of interacting brain regions.