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David M. Schmidt

Publications and source records attributed to David M. Schmidt.

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Continuous Probability Distributions from Finite Data

Recent approaches to the problem of inferring a continuous probability distribution from a finite set of data have used a scalar field theory for the form of the prior probability distribution. This letter presents a more general form for the prior distribution that has a geometrical interpretation which is useful for tailoring prior distributions to the needs of each application. Examples are presented that demonstrate some of the capabilities of this approach, including the applicability of this approach to problems of more than one dimension.

physics.data-an

Bayesian Inference Applied to the Electromagnetic Inverse Problem

We present a new approach to the electromagnetic inverse problem that explicitly addresses the ambiguity associated with its ill-posed character. Rather than calculating a single ``best'' solution according to some criterion, our approach produces a large number of likely solutions that both fit the data and any prior information that is used. While the range of the different likely results is representative of the ambiguity in the inverse problem even with prior information present, features that are common across a large number of the different solutions can be identified and are associated with a high degree of probability. This approach is implemented and quantified within the formalism of Bayesian inference which combines prior information with that from measurement in a common framework using a single measure. To demonstrate this approach, a general neural activation model is constructed that includes a variable number of extended regions of activation and can incorporate a great deal of prior information on neural current such as information on location, orientation, strength and spatial smoothness. Taken together, this activation model and the Bayesian inferential approach yield estimates of the probability distributions for the number, location, and extent of active regions. Both simulated MEG data and data from a visual evoked response experiment are used to demonstrate the capabilities of this approach.

q-bio.NC