ArticlePLoS computational biology2025
Predicting neuronal firing from calcium imaging using a control theoretic approach.
Article in PLoS computational biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
2 citing papers in PubMed.
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
Calcium imaging techniques, such as two-photon imaging, have become a powerful tool to explore the functions of neurons and the connectivity of their circuitry. Frequently, fluorescent calcium indicators are taken as a direct measure of neuronal activity. These indicators, however, are slow relative to behavior, obscuring functional relationships between an animal's movements and the true neuronal activity. As a consequence, the firing rate of a neuron is a more meaningful metric. Converting calcium imaging data to the firing of a neuron is nontrivial. Most state-of-the-art methods depend largely on non-mechanistic modeling frameworks such as neural networks, which do not illuminate the underlying chemical exchanges within the neuron, require significant data to be trained on, and cannot be implemented in real-time. Leveraging modeling frameworks from chemical reaction networks (CRN) coupled with a control theoretic approach, a new algorithm is presented leveraging a fully deterministic ordinary differential equation (ODE) model. This framework utilizes model predictive control (MPC) to challenge state-of-the-art correlation scores while retaining interpretability. Furthermore, these computations can be done in real time, thus, enabling online experimentation informed by neuronal firing rates. To demonstrate the use cases of this architecture, it is tested on ground truth datasets courtesy of the spikefinder challenge. Finally, we propose potential applications of the model for guiding experimental design.
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Registered trials
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.