arXiv subjects

Eviatar Yemini

Publications and source records attributed to Eviatar Yemini.

3 recordsLinked to original sources

arXiv2026

Inferring Active Neural Circuits Using Diffusion Scores

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.

q-bio.NC↗

arXiv2024

The time is ripe to reverse engineer an entire nervous system: simulating behavior from neural interactions

Just like electrical engineers understand how microprocessors execute programs in terms of how transistor currents are affected by their inputs, neuroscientists want to understand behavior production in terms of how neuronal outputs are affected by their inputs and internal states. This dependency of neuronal outputs on inputs can be described by a state-dependent input-output (IO)-function. However, to reliably identify these IO-functions, we need to perturb each input and combinations of inputs while observing all the outputs. Here, we argue that such completeness is possible in C. elegans; a complete description that goes all the way from the activity of every neuron to predict behavior. The established and growing toolkit of optophysiology can non-invasively capture and control every neuron's activity and scale to countless experiments. The information from many such experiments can be pooled while capturing the inter-individual variability because neuronal identity and function are largely conserved across individuals. Just like electrical engineers use transistor IO-functions to simulate program execution, we argue that neuronal IO-functions could be used to simulate the impressive breadth of brain states and behaviors of C. elegans.

q-bio.NC↗

arXiv2024

Learning dynamic representations of the functional connectome in neurobiological networks

The static synaptic connectivity of neuronal circuits stands in direct contrast to the dynamics of their function. As in changing community interactions, different neurons can participate actively in various combinations to effect behaviors at different times. We introduce an unsupervised approach to learn the dynamic affinities between neurons in live, behaving animals, and to reveal which communities form among neurons at different times. The inference occurs in two major steps. First, pairwise non-linear affinities between neuronal traces from brain-wide calcium activity are organized by non-negative tensor factorization (NTF). Each factor specifies which groups of neurons are most likely interacting for an inferred interval in time, and for which animals. Finally, a generative model that allows for weighted community detection is applied to the functional motifs produced by NTF to reveal a dynamic functional connectome. Since time codes the different experimental variables (e.g., application of chemical stimuli), this provides an atlas of neural motifs active during separate stages of an experiment (e.g., stimulus application or spontaneous behaviors). Results from our analysis are experimentally validated, confirming that our method is able to robustly predict causal interactions between neurons to generate behavior. Code is available at https://github.com/dyballa/dynamic-connectomes.

q-bio.NC↗