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Christof Fehrman

Publications and source records attributed to Christof Fehrman.

3 recordsLinked to original sources

Learning Time-Varying Connectomes for Stable Behavior Across Development

Neural circuits must maintain functionality to drive effective behavior while their size, topology, geometry, and intrinsic dynamics change across development. To model developing visuomotor circuits and behavior, we investigated whether a single compact generative encoding could produce functional recurrent controllers across such changes. Building on the HyperNEAT algorithm, we represented this program as a compositional pattern-producing network that received developmental time as an input to generate age-specific connectivity. The developmental substrate prescribed neuronal birth, position, sensory organization, and intrinsic time constants. We tested this approach using two geometrically distinct developmental substrates and two visuomotor tasks: optomotor responses and phototaxis. Controllers optimized at only the initial or mature substrate generally failed when evaluated at other ages. In contrast, controllers optimized across multiple developmental snapshots maintained substantially higher and more consistent performance across trained and unseen ages. Optimization at only three developmental snapshots was often sufficient to produce effective behavior across the tested developmental interval. The resulting connectomes changed substantially with age and did not converge on a single trajectory of sparsity or connection-weight statistics. Controllers also differed in whether they relied on neurons born later in development. These results demonstrate that a shared spatiotemporal time-varying connectivity program can produce recurrent neural networks that preserve behavior across substantial developmental changes. Together, these results provide a framework for studying how functional stability can emerge without requiring structural or dynamical stability.

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Model Predictive Control on the Neural Manifold

Neural manifolds are an attractive theoretical framework for characterizing the complex behaviors of neural populations. However, many of the tools for identifying these low-dimensional subspaces are correlational and provide limited insight into the underlying dynamics. The ability to precisely control the latent activity of a circuit would allow researchers to investigate the structure and function of neural manifolds. We simulate controlling the latent dynamics of a neural population using closed-loop, dynamically generated sensory inputs. Using a spiking neural network (SNN) as a model of a neural circuit, we find low-dimensional representations of both the network activity (the neural manifold) and a set of salient visual stimuli. The fields of classical and optimal control offer a range of methods to choose from for controlling dynamics on the neural manifold, which differ in performance, computational cost, and ease of implementation. Here, we focus on two commonly used control methods: proportional-integral-derivative (PID) control and model predictive control (MPC). PID is a computationally lightweight controller that is simple to implement. In contrast, MPC is a model-based, anticipatory controller with a much higher computational cost and engineering overhead. We evaluate both methods on trajectory-following tasks in latent space, under partial observability and in the presence of unknown noise. While both controllers in some cases were able to successfully control the latent dynamics on the neural manifold, MPC consistently produced more accurate control and required less hyperparameter tuning. These results demonstrate how MPC can be applied on the neural manifold using data-driven dynamics models, and provide a framework to experimentally test for causal relationships between manifold dynamics and external stimuli.

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Nonlinear Model Predictive Control of a Conductance-Based Neuron Model via Data-Driven Forecasting

Objective. Precise control of neural systems is essential to experimental investigations of how the brain controls behavior and holds the potential for therapeutic manipulations to correct aberrant network states. Model predictive control, which employs a dynamical model of the system to find optimal control inputs, has promise for dealing with the nonlinear dynamics, high levels of exogenous noise, and limited information about unmeasured states and parameters that are common in a wide range of neural systems. However, the challenge still remains of selecting the right model, constraining its parameters, and synchronizing to the neural system. Approach. As a proof of principle, we used recent advances in data-driven forecasting to construct a nonlinear machine-learning model of a Hodgkin-Huxley type neuron when only the membrane voltage is observable and there are an unknown number of intrinsic currents. Main Results. We show that this approach is able to learn the dynamics of different neuron types and can be used with MPC to force the neuron to engage in arbitrary, researcher-defined spiking behaviors. Significance. To the best of our knowledge, this is the first application of nonlinear MPC of a conductance-based model where there is only realistically limited information about unobservable states and parameters.

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