BRIDGE provides a reproducible foundation for developing biologically informed mean-field models suitable for large-scale and whole-brain simulations, supporting the transition from generic homogeneous population models toward region-specific ones.
Abstract
Mean-field models are extensively used in large-scale brain simulations because they provide a wieldy description of population dynamics while preserving key features of neural activity. Despite their widespread adoption, no common and reproducible methodology currently exists to systematically derive and validate mean-field models starting from biologically grounded single neuron dynamics. As a result, implementations are often ad hoc, difficult to reproduce and rarely reusable. Here we introduce BRIDGE, a modular, open-source Python pipeline that enables the bottom-up reconstruction, analysis, validation, and simulation of mean-field models from single neurons. The framework integrates single neurons modelling, network simulations, extraction of population statistics, parameters analysis, quantitative comparisons between spiking neural networks and corresponding mean-field representations, and simulation of network of mean-fields. Its flexible architecture allows users to incorporate different neuron models and to generate region-specific or state-dependent mean-field formulations. BRIDGE provides a reproducible foundation for developing biologically informed mean-field models suitable for large-scale and whole-brain simulations, supporting the transition from generic homogeneous population models toward region-specific ones. Graphical abstract
The pipeline is an accessible, transparent tool for fitting biophysically detailed network models, turning parameter identifiability into a routine output; the basal ganglia result is a proof-of-concept rather than a mechanistic claim about pathological beta.
K. Ranak, William S. Anderson· Journal of Neural Engineerin...· 0 citations
Whole-brain transcriptomic atlases are now widely available, yet computational neural models are almost exclusively parameterized from rodent data and used to infer human brain function, an extrapolation whose cost remains unquantified. To address this, we constructed a biophysically detailed, conductance-based Hodgkin...
This review asks which microscopic mechanisms remain explicit, interpretable, and testable after reduction, and what claims these models support, using receptor-aware adaptive mean fields from the master-equation lineage as a worked case.
Yannaël Bossard, Lehna Bekri, A. Destexhe· 0 citations
Multi-compartment Hodgkin-Huxley (HH) models provide a principled framework for predicting neural dynamics and responses to electrical stimulation. However, fitting HH biophysical parameters typically requires intracellular recordings, which are invasive and low-throughput, limiting the ability to capture the geometry...
A. Lotlikar, Ian-Christopher Tanoh, Praful K. Vasireddy et al.· 0 citations
A GUI-based tool, NeuronOpt, was implemented on the workflow improving the accessibility and repeatability of the approach and allowing the method reusable beyond cerebellar neurons, and the methodology allow computational reliability of the hybrid optimization framework to be used for optimization across multiple appl...
Radhika Shrimankar, Asha Vijayan, Giovanni Naldi et al.· IEEE Access· 0 citations
It is found that the method alone can change the apparent structure of the network as much as real biological differences do, and practical recommendations for parameter selection, reporting, and cross-method validation in MEA-based network neuroscience are provided.
J. Ort, V. Witzig, Aniella Bak et al.· bioRxiv· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.