Benchmarking Probabilistic Time Series Forecasting Models on Neural Activity
Ziyu Lu, Anna J. Li, Alexander E. Ladd, Pascha Matveev, Aditya Deole, Eric Shea-Brown, J. Nathan Kutz, Nicholas A. Steinmetz
TL;DR
This work addresses forecasting neural activity with probabilistic, uncertainty-aware predictions by benchmarking eight probabilistic deep learning models (including two foundation models) and four classical baselines on spontaneous widefield calcium imaging data from mouse cortex. It finds that deep models such as PatchTST, TiDE, and fine-tuned Chronos consistently outperform baselines across multiple forecast horizons, while zero-shot transfers for Chronos and Moirai underperform until fine-tuned. Informative forecasts extend up to about $1.5$ seconds into the future, with reliability highest near $1$ second ($\approx 35$ steps) and diminishing beyond $1.5$ seconds, as uncertainty grows and predictions resemble the training distribution mean. These results motivate the development of neuroscience-focused forecasting foundations and underscore the value of uncertainty quantification for potential closed-loop neural control applications, while also highlighting intrinsic neural variability as a limiting factor.
Abstract
Neural activity forecasting is central to understanding neural systems and enabling closed-loop control. While deep learning has recently advanced the state-of-the-art in the time series forecasting literature, its application to neural activity forecasting remains limited. To bridge this gap, we systematically evaluated eight probabilistic deep learning models, including two foundation models, that have demonstrated strong performance on general forecasting benchmarks. We compared them against four classical statistical models and two baseline methods on spontaneous neural activity recorded from mouse cortex via widefield imaging. Across prediction horizons, several deep learning models consistently outperformed classical approaches, with the best model producing informative forecasts up to 1.5 seconds into the future. Our findings point toward future control applications and open new avenues for probing the intrinsic temporal structure of neural activity.
