Search arXiv⌕ Search

arXiv · 2609.35207

High-rank connectivity scaffolds support precision and generalisation in recurrent neural networks

Abstract

A major challenge in neuroscience and machine learning is to connect single-neuron influence, population dynamics, and circuit connectivity in a causal account of computation. Much previous work has shown that low-rank connectivity can generate low-dimensional dynamics in trained artificial neural networks, but this leaves unclear the functional relevance of the higher-rank structure of biological neural circuits and many artificial neuronal networks. Here we analyse recurrent neural networks trained to locate rewards by integrating continuously varying speed inputs in one- and two-dimensional spatial tasks. We find that dominant low-dimensional dynamics encode task locations, and can be causally manipulated to instruct behavioural outcomes. However, after decomposing the underlying circuitry we found that while low-rank connectivity accounts for the low-dimensional dynamics, accurate performance and generalisation to novel speed distributions requires high-rank connectivity. We demonstrate that this is achieved through distributed signalling that corrects errors in low-dimensional location representations. Thus, combined perturbation-, representation-, and circuit-level analyses demonstrate a novel mechanism for robust spatial computation and show how high-rank connectivity in neural circuits can provide a scaffold that supports precision and generalisation.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Ian Hawes, Matt Nolan. 2026-09-28. High-rank connectivity scaffolds support precision and generalisation in recurrent neural networks. https://arxiv.org/abs/2609.35207

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Neural spikes as rare events

We consider the information transmission problem in neurons and its possible implications for learning in neural networks. Our approach is based on recent developments in statistical physics and complexity science. Combining sensory information from various modalities for perceptual decision-making offers several advantages and is essential for the survival of both humans and animals. Not much is known about which brain regions are involved in spatial localization using audiovisual integration. We explore this further by training mice in a task requiring audiovisual integration. We then record from the secondary motor cortex (M2) using high-density electrophysiology. Analyzing this data, we found neurons responsive to multimodal as well as unimodal auditory and visual stimuli. The neurons are generally more responsive to auditory, rather than visual, stimuli. There was low correlation between the auditory and visual responses. Some neurons were sensitive to the task mode, whether active or passive, with more neurons being responsive in the active mode. A relatively large percentage of neurons (10-11%) differed significantly in their response to left and right-sided auditory stimuli, but only in 1 of the 3 mice we recorded from. These findings suggest a role for M2 in multisensory decision making and should enable further research in this field. We then use branching process simulations to model neural activity. This would support temporal coding theory as a model for neural coding.

q-bio.NC↗

Association profile conditioning in a set-temporal transformer for cross-session intracortical motor decoding

Intracortical motor decoders degrade across sessions because the set of recorded units changes and persisting units can alter how their firing relates to behavior. Most existing methods update network weights on each new session or rely on unlabeled activity, which does not directly reveal such changes. We present APST, an Association Profile-conditioned Set-Temporal transformer that adapts to new sessions with all network weights frozen. From a few labeled calibration trials, APST summarizes how each unit's firing relates to behavior in a four-dimensional association profile computed in closed form. The profiles condition a set-attention encoder that accepts any number and order of units, followed by a causal transformer for streaming decoding. On held-out DANDI688 sessions from two monkeys, APST reaches velocity $R^2$ of $0.78$ and $0.81$, versus $0.40$ and $0.58$ for a variant that uses neural activity alone, and matches or exceeds an RNN fine-tuned on the same trials. On FALCON private held-out evaluation, it attains $R^2$ of $0.65$, $0.42$, and $0.44$ on M1, M2, and H1.

q-bio.NC↗

BrainWave: A Brain Signal Foundation Model for Clinical Applications

Neural electrical activity is fundamental to brain function, underlying a range of cognitive and behavioral processes, including movement, perception, decision-making, and consciousness. Abnormal patterns of neural signaling often indicate the presence of underlying brain diseases. The variability among individuals, the diverse array of clinical symptoms from various brain disorders, and the limited availability of diagnostic classifications, have posed significant barriers to formulating reliable model of neural signals for diverse application contexts. Here, we present BrainWave, the first foundation model for both invasive and non-invasive neural recordings, pretrained on more than 40,000 hours of electrical brain recordings (13.79 TB of data) from approximately 16,000 individuals. Our analysis show that BrainWave outperforms all other competing models and consistently achieves state-of-the-art performance in the diagnosis and identification of neurological disorders. We also demonstrate robust capabilities of BrainWave in enabling zero-shot transfer learning across varying recording conditions and brain diseases, as well as few-shot classification without fine-tuning, suggesting that BrainWave learns highly generalizable representations of neural signals. We hence believe that open-sourcing BrainWave will facilitate a wide range of clinical applications in medicine, paving the way for AI-driven approaches to investigate brain disorders and advance neuroscience research.

q-bio.NC↗