Evidence map›Paper›PMID 40502138›Full record

ArticlebioRxiv : the preprint server for biology2025

Machine Learning Discovers Numerous New Computational Principles Supporting Elementary Motion Detection.

Alon Poleg-Polsky

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.

0numbers the graph read from it
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

1 author.

Alon Poleg-PolskyDepartment of Physiology and Biophysics, and Neuroscience Program, University of Colorado School of Medicine, Aurora, CO 80045, USA.ORCID 0000-0003-1327-5129

Funding

Mechanisms of direction selectivity in starburst amacrine cellsR01EY030841 · NEI · UNIVERSITY OF COLORADO DENVER · PI POLEG-POLSKY, ALON · 2020 to 2024
$1.9M
Novel experimental and machine learning - assisted techniques to assess receptive field functionality in the retinaR01EY035293 · NEI · UNIVERSITY OF COLORADO DENVER · PI Alon Poleg-Polsky · 2023 to 2026
$1.9M
NEI NIH HHS R01 EY030841NEI NIH HHS R01 EY035293
6 · The paper itself

Abstract

Motion direction detection is a fundamental visual computation that transforms spatial luminance patterns into directionally tuned outputs. Classical models of direction selectivity rely on temporal asymmetry, where motion detection arises through either delayed excitation or inhibition. Here, I used biologically inspired machine learning applied to retinal and cortical circuits to uncover multiple novel feedforward architectures capable of direction selectivity. These include mechanisms based on asymmetric synaptic properties, spatial receptive field variations, new roles for pre- and postsynaptic inhibition, and previously unrecognized kinetic implementations. Conceptually, these circuit architectures cluster into eight computational primitives underlying motion detection, four of which are newly discovered. Many of the solutions rival or outperform classical models in both robustness and precision, and several exhibit enhanced noise tolerance. All mechanisms are biologically plausible and correspond to known physiological and anatomical motifs, offering fresh insights into motion processing and illustrating how machine learning can uncover general principles of neural computation.

Identifiers

PMID40502138
PMCPMC12154669

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Registered trials

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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.