ArticlePloS one2026
A genetic algorithm for self-supervised models of oscillatory neurodynamics.
Article in PloS one, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
1 citing paper in PubMed.
- Population-scale analysis of frequency-dependent calcium dynamics in retinal ganglion cells under electric field stimulation.Scientific reports · 2026Article
Corrections and comments
- Update of
Authors and funding
3 authors.
Funding
Abstract
Predictive processing theories propose that the brain builds internal models of its environment by reducing the discrepancy between internally generated predictions and external sensory signals. Prior work has linked these processes to oscillatory activity in gamma (40-100 Hz) and alpha/beta (10-30 Hz) frequency ranges. Current computational approaches face a trade-off: abstract predictive-processing models can implement self-supervised computations but often omit oscillatory spiking dynamics, whereas biophysically constrained spiking models can generate neural rhythms but often require extensive manual tuning. Here, we introduce the Genetic Stochastic Delta Rule (GSDR), an evolutionary optimization framework for fitting nonlinear neural models to electrophysiological objectives. We first evaluate GSDR in simplified optimization settings, then apply it to spiking-network objectives involving firing rates, beta/gamma spectral ratios, and empirical macaque stimulus-evoked gamma dynamics from visual cortex. We show that GSDR can search constrained synaptic parameter spaces, reduce reliance on manual tuning, and reproduce spectral and circuit-level phenotypes associated with predictive routing. We also used Izhikevich simulations as a model-class robustness analysis, showing that the approach is not limited to the original Hodgkin-Huxley-style implementation. These results position GSDR as a methodological framework for automated, multi-objective exploration of oscillatory neural models, with predictive routing serving as a motivating case study rather than as a completed functional proof.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.