Evidence map›Paper›PMID 39868098›Full record

ArticlebioRxiv : the preprint server for biology2025

CONSTRUCTING BIOLOGICALLY CONSTRAINED RNNS VIA DALE'S BACKPROP AND TOPOLOGICALLY-INFORMED PRUNING.

Aishwarya H Balwani, Alex Q Wang, Farzaneh Najafi, Hannah Choi

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Aishwarya H BalwaniSchool of Electrical & Computer Engineering, Georgia Institute of Technology.ORCID 0000-0002-9234-1632
Alex Q WangComputational Science and Engineering Program, Georgia Institute of Technology.ORCID 0009-0005-9628-4910
Farzaneh NajafiSchool of Biological Sciences, Georgia Institute of Technology.ORCID 0000-0001-6454-2448
Hannah ChoiSchool of Mathematics, Georgia Institute of Technology.ORCID 0000-0002-8192-1121

Funding

Bridging structure, dynamics, and information processing in brain networksR00EY030840 · NEI · GEORGIA INSTITUTE OF TECHNOLOGY · PI CHOI, HANNAH · 2021 to 2023
$710k
NEI NIH HHS R00 EY030840
6 · The paper itself

Abstract

Recurrent neural networks (RNNs) have emerged as a prominent tool for modeling cortical function, and yet their conventional architecture is lacking in physiological and anatomical fidelity. In particular, these models often fail to incorporate two crucial biological constraints: i) Dale's law, i.e., sign constraints that preserve the "type" of projections from individual neurons, and ii) Structured connectivity motifs, i.e., highly sparse yet defined connections amongst various neuronal populations. Both constraints are known to impair learning performance in artificial neural networks, especially when trained to perform complicated tasks; but as modern experimental methodologies allow us to record from diverse neuronal populations spanning multiple brain regions, using RNN models to study neuronal interactions without incorporating these fundamental biological properties raises questions regarding the validity of the insights gleaned from them. To address these concerns, our work develops methods that let us train RNNs which respect Dale's law whilst simultaneously maintaining a specific sparse connectivity pattern across the entire network. We provide mathematical grounding and guarantees for our approaches incorporating both types of constraints, and show empirically that our models match the performance of RNNs trained without any constraints. Finally, we demonstrate the utility of our methods for inferring multi-regional interactions by training RNN models of the cortical network to reconstruct 2-photon calcium imaging data during visual behaviour in mice, whilst enforcing data-driven, cell-type specific connectivity constraints between various neuronal populations spread across multiple cortical layers and brain areas. In doing so, we find that the interactions inferred by our model corroborate experimental findings in agreement with the theory of predictive coding, thus validating the applicability of our methods.

Identifiers

PMID39868098
PMCPMC11760306

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.