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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2020
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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. |
format | Online Article Text |
id | pubmed-7728401 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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