ArticleScientific reports2018
Optimal neural inference of stimulus intensities.
Article in Scientific reports, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.
What it found
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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
3 citing papers in PubMed.
- Martingales and the fixation time of evolutionary graphs with arbitrary dimensionality.Royal Society open science · 2022Article
- Neuroregeneration and plasticity: a review of the physiological mechanisms for achieving functional recovery postinjury.Military Medical Research · 2020Review
- The self-organized learning of noisy environmental stimuli requires distinct phases of plasticity.Network neuroscience (Cambridge, Mass.) · 2020Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
Abstract
In natural data, the class and intensity of stimuli are correlated. Current machine learning algorithms ignore this ubiquitous statistical property of stimuli, usually by requiring normalized inputs. From a biological perspective, it remains unclear how neural circuits may account for these dependencies in inference and learning. Here, we use a probabilistic framework to model class-specific intensity variations, and we derive approximate inference and online learning rules which reflect common hallmarks of neural computation. Concretely, we show that a neural circuit equipped with specific forms of synaptic and intrinsic plasticity (IP) can learn the class-specific features and intensities of stimuli simultaneously. Our model provides a normative interpretation of IP as a critical part of sensory learning and predicts that neurons can represent nontrivial input statistics in their excitabilities. Computationally, our approach yields improved statistical representations for realistic datasets in the visual and auditory domains. In particular, we demonstrate the utility of the model in estimating the contrastive stress of speech.
Identifiers
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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.