Pith. sign in

Learning Time-Varying Multi-Region Brain Communications via Scalable Markovian Gaussian Processes

1 Pith paper cite this work. Polarity classification is still indexing.

1 Pith paper citing it
abstract

Understanding and constructing brain communications that capture dynamic communications across multiple regions is fundamental to modern system neuroscience, yet current methods struggle to find time-varying region-level communications or scale to large neural datasets with long recording durations. We present a novel framework using Markovian Gaussian Processes to learn brain communications with time-varying temporal delays from multi-region neural recordings, named Adaptive Delay Model (ADM). Our method combines Gaussian Processes with State Space Models and employs parallel scan inference algorithms, enabling efficient scaling to large datasets while identifying concurrent communication patterns that evolve over time. This time-varying approach captures how brain region interactions shift dynamically during cognitive processes. Validated on synthetic and multi-region neural recordings datasets, our approach discovers both the directionality and temporal dynamics of neural communication. This work advances our understanding of distributed neural computation and provides a scalable tool for analyzing dynamic brain networks.

fields

stat.ML 1

years

2024 1

verdicts

CONDITIONAL 1

representative citing papers

Fast Multi-Group Gaussian Process Factor Models

stat.ML · 2024-12-21 · conditional · novelty 7.0

Introduces inducing-variable and frequency-domain approximations for multi-group Gaussian process factor models, achieving linear scaling in trial length and group count with minimal accuracy loss.

citing papers explorer

Showing 1 of 1 citing paper.

  • Fast Multi-Group Gaussian Process Factor Models stat.ML · 2024-12-21 · conditional · none · ref 38 · internal anchor

    Introduces inducing-variable and frequency-domain approximations for multi-group Gaussian process factor models, achieving linear scaling in trial length and group count with minimal accuracy loss.