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Interpretation of correlated neural variability from models of feed-forward and recurrent circuits
Neural populations respond to the repeated presentations of a sensory stimulus with correlated variability. These correlations have been studied in detail, with respect to their mechanistic origin, as well as their influence on stimulus discrimination and on the performance of population codes. A nu...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833435/ https://www.ncbi.nlm.nih.gov/pubmed/29408930 http://dx.doi.org/10.1371/journal.pcbi.1005979 |
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author | Pernice, Volker da Silveira, Rava Azeredo |
author_facet | Pernice, Volker da Silveira, Rava Azeredo |
author_sort | Pernice, Volker |
collection | PubMed |
description | Neural populations respond to the repeated presentations of a sensory stimulus with correlated variability. These correlations have been studied in detail, with respect to their mechanistic origin, as well as their influence on stimulus discrimination and on the performance of population codes. A number of theoretical studies have endeavored to link network architecture to the nature of the correlations in neural activity. Here, we contribute to this effort: in models of circuits of stochastic neurons, we elucidate the implications of various network architectures—recurrent connections, shared feed-forward projections, and shared gain fluctuations—on the stimulus dependence in correlations. Specifically, we derive mathematical relations that specify the dependence of population-averaged covariances on firing rates, for different network architectures. In turn, these relations can be used to analyze data on population activity. We examine recordings from neural populations in mouse auditory cortex. We find that a recurrent network model with random effective connections captures the observed statistics. Furthermore, using our circuit model, we investigate the relation between network parameters, correlations, and how well different stimuli can be discriminated from one another based on the population activity. As such, our approach allows us to relate properties of the neural circuit to information processing. |
format | Online Article Text |
id | pubmed-5833435 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-58334352018-03-23 Interpretation of correlated neural variability from models of feed-forward and recurrent circuits Pernice, Volker da Silveira, Rava Azeredo PLoS Comput Biol Research Article Neural populations respond to the repeated presentations of a sensory stimulus with correlated variability. These correlations have been studied in detail, with respect to their mechanistic origin, as well as their influence on stimulus discrimination and on the performance of population codes. A number of theoretical studies have endeavored to link network architecture to the nature of the correlations in neural activity. Here, we contribute to this effort: in models of circuits of stochastic neurons, we elucidate the implications of various network architectures—recurrent connections, shared feed-forward projections, and shared gain fluctuations—on the stimulus dependence in correlations. Specifically, we derive mathematical relations that specify the dependence of population-averaged covariances on firing rates, for different network architectures. In turn, these relations can be used to analyze data on population activity. We examine recordings from neural populations in mouse auditory cortex. We find that a recurrent network model with random effective connections captures the observed statistics. Furthermore, using our circuit model, we investigate the relation between network parameters, correlations, and how well different stimuli can be discriminated from one another based on the population activity. As such, our approach allows us to relate properties of the neural circuit to information processing. Public Library of Science 2018-02-06 /pmc/articles/PMC5833435/ /pubmed/29408930 http://dx.doi.org/10.1371/journal.pcbi.1005979 Text en © 2018 Pernice, da Silveira http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pernice, Volker da Silveira, Rava Azeredo Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title | Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title_full | Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title_fullStr | Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title_full_unstemmed | Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title_short | Interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
title_sort | interpretation of correlated neural variability from models of feed-forward and recurrent circuits |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5833435/ https://www.ncbi.nlm.nih.gov/pubmed/29408930 http://dx.doi.org/10.1371/journal.pcbi.1005979 |
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