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Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data

The pattern of neural activity evoked by a stimulus can be substantially affected by ongoing spontaneous activity. Separating these two types of activity is particularly important for calcium imaging data given the slow temporal dynamics of calcium indicators. Here we present a statistical model tha...

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Autores principales: Triplett, Marcus A., Pujic, Zac, Sun, Biao, Avitan, Lilach, Goodhill, Geoffrey J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728401/
https://www.ncbi.nlm.nih.gov/pubmed/33253161
http://dx.doi.org/10.1371/journal.pcbi.1008330
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author Triplett, Marcus A.
Pujic, Zac
Sun, Biao
Avitan, Lilach
Goodhill, Geoffrey J.
author_facet Triplett, Marcus A.
Pujic, Zac
Sun, Biao
Avitan, Lilach
Goodhill, Geoffrey J.
author_sort Triplett, Marcus A.
collection PubMed
description The pattern of neural activity evoked by a stimulus can be substantially affected by ongoing spontaneous activity. Separating these two types of activity is particularly important for calcium imaging data given the slow temporal dynamics of calcium indicators. Here we present a statistical model that decouples stimulus-driven activity from low dimensional spontaneous activity in this case. The model identifies hidden factors giving rise to spontaneous activity while jointly estimating stimulus tuning properties that account for the confounding effects that these factors introduce. By applying our model to data from zebrafish optic tectum and mouse visual cortex, we obtain quantitative measurements of the extent that neurons in each case are driven by evoked activity, spontaneous activity, and their interaction. By not averaging away potentially important information encoded in spontaneous activity, this broadly applicable model brings new insight into population-level neural activity within single trials.
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spelling pubmed-77284012020-12-17 Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data Triplett, Marcus A. Pujic, Zac Sun, Biao Avitan, Lilach Goodhill, Geoffrey J. PLoS Comput Biol Research Article The pattern of neural activity evoked by a stimulus can be substantially affected by ongoing spontaneous activity. Separating these two types of activity is particularly important for calcium imaging data given the slow temporal dynamics of calcium indicators. Here we present a statistical model that decouples stimulus-driven activity from low dimensional spontaneous activity in this case. The model identifies hidden factors giving rise to spontaneous activity while jointly estimating stimulus tuning properties that account for the confounding effects that these factors introduce. By applying our model to data from zebrafish optic tectum and mouse visual cortex, we obtain quantitative measurements of the extent that neurons in each case are driven by evoked activity, spontaneous activity, and their interaction. By not averaging away potentially important information encoded in spontaneous activity, this broadly applicable model brings new insight into population-level neural activity within single trials. Public Library of Science 2020-11-30 /pmc/articles/PMC7728401/ /pubmed/33253161 http://dx.doi.org/10.1371/journal.pcbi.1008330 Text en © 2020 Triplett et al 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
Triplett, Marcus A.
Pujic, Zac
Sun, Biao
Avitan, Lilach
Goodhill, Geoffrey J.
Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title_full Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title_fullStr Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title_full_unstemmed Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title_short Model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
title_sort model-based decoupling of evoked and spontaneous neural activity in calcium imaging data
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7728401/
https://www.ncbi.nlm.nih.gov/pubmed/33253161
http://dx.doi.org/10.1371/journal.pcbi.1008330
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