Maximum likelihood estimation of spatially dependent interactions in large populations of cortical neurons

Understanding how functional connectivity between cortical neurons varies with spatial distance is crucial for characterizing large-scale neural dynamics. However, inferring these spatial patterns is challenging when spike trains are collected from large populations of neurons. Here, we present a maximum likelihood estimation (MLE) framework to quantify distance-dependent functional interactions directly from observed spiking activity. We validate this method using both synthetic spike trains generated from a linear Poisson model and biologically realistic simulations performed with Izhikevich neurons. We then apply the approach to large-scale electrophysiological recordings from V1 cortical neurons. Our results show that the proposed MLE approach robustly captures spatial decay in functional connectivity, providing insights into the spatial structure of population-level neural interactions.

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Publication Details

Journal
Frontiers in Computational Neuroscience
Published
2025-08-13
DOI
https://doi.org/10.3389/fncom.2025.1639829
Primary Topic
Neural dynamics and brain function
Type
article
Field-Weighted Citation Impact
0.00

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article

Maximum likelihood estimation of spatially dependent interactions in large populations of cortical neurons

Jean‐Philippe Thivierge, C. Godin
Frontiers in Computational Neuroscience
Neural dynamics and brain function
article

Maximum likelihood estimation of spatially dependent interactions in large populations of cortical neurons

Jean‐Philippe Thivierge, C. Godin
article en

Abstract

Understanding how functional connectivity between cortical neurons varies with spatial distance is crucial for characterizing large-scale neural dynamics. However, inferring these spatial patterns is challenging when spike trains are collected from large populations of neurons. Here, we present a maximum likelihood estimation (MLE) framework to quantify distance-dependent functional interactions directly from observed spiking activity. We validate this method using both synthetic spike trains generated from a linear Poisson model and biologically realistic simulations performed with Izhikevich neurons. We then apply the approach to large-scale electrophysiological recordings from V1 cortical neurons. Our results show that the proposed MLE approach robustly captures spatial decay in functional connectivity, providing insights into the spatial structure of population-level neural interactions.

Frontiers in Computational NeuroscienceVol. 19
University of Ottawa (CA)
Natural Sciences and Engineering Research Council of Canada
Openalex Percentile: Top 80%
Neural dynamics and brain function
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