Uncovering Dynamic Neural Information Flow with Continuous-Time Weighted Dynamic Bayesian Networks

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Abstract

ABSTRACT Understanding how information dynamically flows within neural systems is a crucial problem in neuroscience. Traditional approaches often assume stationary or quasi-stationary functional networks, which fail to capture the time-varying dynamics of interactions among neural variables. To address this limitation, we introduce Continuous-Time weighted Dynamic Bayesian Networks (CTwDBN), a non-stationary graphical modeling framework for uncovering smoothly time-varying conditional dependencies. Validation on synthetic datasets demonstrated that CTwDBN reliably recovers the structure and dynamics of ground-truth information flow. Application to electrophysiological recordings during a guided saccade task revealed temporal fluctuations in conditional dependencies in the cortical network that persisted an order of magnitude longer than the receptive field dynamics. In the resting-state cortex, CTwDBN revealed persistent fluctuations within a low-dimensional dependency space reflecting canonical anatomical motifs. These results highlight CTwDBN as a versatile analytical framework for capturing dynamic information flow in neural systems with broad applicability to complex biological and artificial systems.
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ABSTRACT Understanding how information dynamically flows within neural systems is a crucial problem in neuroscience. Traditional approaches often assume stationary or quasi-stationary functional networks, which fail to capture the time-varying dynamics of interactions among neural variables. To address this limitation, we introduce Continuous-Time weighted Dynamic Bayesian Networks (CTwDBN), a non-stationary graphical modeling framework for uncovering smoothly time-varying conditional dependencies. Validation on synthetic datasets demonstrated that CTwDBN reliably recovers the structure and dynamics of ground-truth information flow. Application to electrophysiological recordings during a guided saccade task revealed temporal fluctuations in conditional dependencies in the cortical network that persisted an order of magnitude longer than the receptive field dynamics. In the resting-state cortex, CTwDBN revealed persistent fluctuations within a low-dimensional dependency space reflecting canonical anatomical motifs. These results highlight CTwDBN as a versatile analytical framework for capturing dynamic information flow in neural systems with broad applicability to complex biological and artificial systems. Competing Interest Statement The authors have declared no competing interest. Footnotes ↵† senior authors

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last seen: 2026-05-20T01:45:00.602351+00:00