aiqbench analysis
This research introduces conditional flow matching to model the stochastic variability of single-neuron electrophysiology, overcoming the limitations of deterministic surrogates that map stimuli to single responses. By training on biophysically detailed models, the method successfully reproduces complex spike-time structures and coexisting firing modes near thresholds, offering a computationally efficient alternative to massive ensemble simulations. This advancement enables more accurate neural network modeling by capturing the full distribution of voltage responses rather than averaging them out.
Conditional Flow Matching for Single-Neuron Electrophysiology: Capturing Multimodal Responses Across Stimuli
arXiv:2610.06520v1 Announce Type: new Abstract: Neurons of the brain exhibit a rich repertoire of electrophysiology dynamics with the same repeated stimulus eliciting very different voltage responses from the same cell. One common approach in biophysically detailed models is to capture this variability through ensembles of deterministic parametrizations, at a cost of hundreds of thousands of CPU hours. Existing machine learning surrogates inherit the same limitation, where a stimulus is mapped to a single voltage response. We address this challenge by learning a conditional generative model for single-neuron electrophysiology, using flow matching with a velocity field conditioned on the input current. On biophysically detailed models of two human cortical interneuron types, the generated responses closely reproduce the electrophysiological feature distributions, spike-time structure, and excitability profiles, even matching the experimental recordings from the corresponding human cortical neurons. Near the firing threshold, firing and non-firing responses coexist at the same stimulus amplitude, and at high amplitudes, ensembles may split into low- and high-firing modes near depolarization block. We show that our model recovers both modes in each case, while a neural operator baseline suppresses spiking near threshold and blurs the gap between modes at depolarization block.
Abstract:Neurons of the brain exhibit a rich repertoire of electrophysiology dynamics with the same repeated stimulus eliciting very different voltage responses from the same cell. One common approach in biophysically detailed models is to capture this variability through ensembles of deterministic parametrizations, at a cost of hundreds of thousands of CPU hours. Existing machine learning surrogates inherit the same limitation, where a stimulus is mapped to a single voltage response. We address this challenge by learning a conditional generative model for single-neuron electrophysiology, using flow matching with a velocity field conditioned on the input current. On biophysically detailed models of two human cortical interneuron types, the generated responses closely reproduce the electrophysiological feature distributions, spike-time structure, and excitability profiles, even matching the experimental recordings from the corresponding human cortical neurons. Near the firing threshold, firing and non-firing responses coexist at the same stimulus amplitude, and at high amplitudes, ensembles may split into low- and high-firing modes near depolarization block. We show that our model recovers both modes in each case, while a neural operator baseline suppresses spiking near threshold and blurs the gap between modes at depolarization block.
Machine Learning (cs.LG)
arXiv:2610.06520 [cs.LG]
(or arXiv:2610.06520v1 [cs.LG] for this version)
https://doi.org/10.48550/arXiv.2610.06520 Focus to learn more arXiv-issued DOI via DataCite (pending registration)
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