ArXiv TLDR

Inferring Active Neural Circuits Using Diffusion Scores

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2605.02852

Savik Kinger, Johannes Bertram, Luciano Dyballa, Eviatar Yemini, Steven W. Zucker

q-bio.NC

TLDR

SBTG infers lag-specific neural circuit interactions from population activity using denoising score models, avoiding parametric assumptions and omitted-lag bias.

Key contributions

  • Introduces Score--Block Time Graphs (SBTG) for inferring directed, lag-specific neural interactions.
  • Leverages denoising score models and cross-block score products to recover transition map Jacobians.
  • Uses multi-block windows to condition on intermediate time points, avoiding omitted-lag bias.
  • Applied to C. elegans data, revealing novel lag-specific circuit structure and improved connectome alignment.

Why it matters

This paper introduces a powerful new method, SBTG, to accurately infer active neural circuits from complex population data. It overcomes limitations of current approaches by avoiding parametric assumptions and omitted-lag bias. This tool can transform high-dimensional neural recordings into testable circuit hypotheses, advancing our understanding of brain function.

Original Abstract

In biological systems, neural circuits compute through directed, short-latency interactions whose effects unfold across multiple time scales and behavioral contexts. We address the problem of inferring these local, lag-specific interactions from sampled neural population activity under varying stimuli, without assuming a parametric form for the underlying dynamics. Our approach leverages denoising score models by estimating joint-window scores over consecutive activity snapshots (i.e., brain states) and converting these scores into calibrated, directed edge tests via cross-block score products. The key insight is that these products recover the Jacobian of the transition map between brain states under nonlinear dynamics. To cleanly separate lag-specific effects, we introduce minimal multi-block windows that condition on intermediate time points, avoiding the omitted-lag bias inherent in pairwise analyses. The resulting method, Score--Block Time Graphs (SBTG), identifies lag-specific directed interactions in sampled neuronal population data. We specifically apply SBTG to whole-brain C. elegans calcium imaging data to recover lag-specific circuit structure not resolved by current methods, including improved alignment with independent connectomes, cell-type-specific temporal organization, and neuromodulatory profiles consistent with known receptor kinetics. These findings highlight the potential for SBTG to serve as a practical ``AI for science'' tool by turning high-dimensional neural population recordings into statistically testable circuit hypotheses.

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