Evidence map›Paper›PMID 42166500›Full record

ArticlePLoS computational biology2026

Fast reconstruction of degenerate populations of conductance-based neuron models from spike times.

Julien Brandoit, Damien Ernst, Guillaume Drion, Arthur Fyon

Abstract read
In one paragraph

Article in PLoS computational biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Julien BrandoitDepartment of Electrical Engineering and Computer Science, University of Liège, Liège, Belgium.ORCID https://orcid.org/0009-0001-2607-4572
Damien ErnstDepartment of Electrical Engineering and Computer Science, University of Liège, Liège, Belgium.
Guillaume DrionDepartment of Electrical Engineering and Computer Science, University of Liège, Liège, Belgium.
Arthur FyonDepartment of Electrical Engineering and Computer Science, University of Liège, Liège, Belgium.ORCID https://orcid.org/0009-0008-0771-8767

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring the biophysical parameters of conductance-based models (CBMs) from experimentally accessible recordings remains a central challenge in computational neuroscience. Spike times are the most widely available data, yet they reveal little about which combinations of ion channel conductances generate the observed activity. This inverse problem is further complicated by neuronal degeneracy, where multiple distinct conductance sets yield similar spiking patterns. We introduce a method that addresses this challenge by combining deep learning with Dynamic Input Conductances (DICs), a theoretical framework that reduces complex CBMs to three interpretable feedback components governing excitability and firing patterns. Our approach first maps spike times directly to DIC densities at threshold using a lightweight neural network that learns a low-dimensional representation of neuronal activity. The predicted DIC values are then used to generate degenerate CBM populations via an iterative compensation algorithm, ensuring compatibility with the intermediate target DICs, and thereby reproducing the corresponding firing patterns, even in high-dimensional models. Applied to two neuronal models, this algorithmic pipeline reconstructs spiking, bursting, and irregular regimes with high accuracy and robustness to variability, including spike trains generated under noisy current injection mimicking physiological stochasticity. It produces diverse degenerate populations within milliseconds on standard hardware, enabling scalable and efficient inference from spike recordings alone. Beyond methodological advances, we provide an open-source software package with a graphical interface that allows experimentalists to generate and explore CBM populations directly from spike trains without requiring programming expertise. Together, this work positions DICs as a practical and interpretable link between experimentally observed activity and mechanistic models. By enabling fast and scalable reconstruction of degenerate populations directly from spike times, our approach provides a powerful way to investigate how neurons exploit conductance variability to achieve reliable computation and provides the foundation for experimental applications that span from neuromodulation studies to real-time model-guided interventions.

Indexed as

Action PotentialsModels, NeurologicalNeuronsAlgorithmsAnimalsComputational BiologyComputer SimulationDeep LearningHumansIon ChannelsNeural Networks, ComputerIon Channels

Identifiers

PMID42166500
PMCPMC13241015

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.