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Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity
Neuronal activity correlations are key to understanding how populations of neurons collectively encode information. While two-photon calcium imaging has created a unique opportunity to record the activity of large populations of neurons, existing methods for inferring correlations from these data fa...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354639/ https://www.ncbi.nlm.nih.gov/pubmed/34180397 http://dx.doi.org/10.7554/eLife.68046 |
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author | Rupasinghe, Anuththara Francis, Nikolas Liu, Ji Bowen, Zac Kanold, Patrick O Babadi, Behtash |
author_facet | Rupasinghe, Anuththara Francis, Nikolas Liu, Ji Bowen, Zac Kanold, Patrick O Babadi, Behtash |
author_sort | Rupasinghe, Anuththara |
collection | PubMed |
description | Neuronal activity correlations are key to understanding how populations of neurons collectively encode information. While two-photon calcium imaging has created a unique opportunity to record the activity of large populations of neurons, existing methods for inferring correlations from these data face several challenges. First, the observations of spiking activity produced by two-photon imaging are temporally blurred and noisy. Secondly, even if the spiking data were perfectly recovered via deconvolution, inferring network-level features from binary spiking data is a challenging task due to the non-linear relation of neuronal spiking to endogenous and exogenous inputs. In this work, we propose a methodology to explicitly model and directly estimate signal and noise correlations from two-photon fluorescence observations, without requiring intermediate spike deconvolution. We provide theoretical guarantees on the performance of the proposed estimator and demonstrate its utility through applications to simulated and experimentally recorded data from the mouse auditory cortex. |
format | Online Article Text |
id | pubmed-8354639 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-83546392021-08-11 Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity Rupasinghe, Anuththara Francis, Nikolas Liu, Ji Bowen, Zac Kanold, Patrick O Babadi, Behtash eLife Neuroscience Neuronal activity correlations are key to understanding how populations of neurons collectively encode information. While two-photon calcium imaging has created a unique opportunity to record the activity of large populations of neurons, existing methods for inferring correlations from these data face several challenges. First, the observations of spiking activity produced by two-photon imaging are temporally blurred and noisy. Secondly, even if the spiking data were perfectly recovered via deconvolution, inferring network-level features from binary spiking data is a challenging task due to the non-linear relation of neuronal spiking to endogenous and exogenous inputs. In this work, we propose a methodology to explicitly model and directly estimate signal and noise correlations from two-photon fluorescence observations, without requiring intermediate spike deconvolution. We provide theoretical guarantees on the performance of the proposed estimator and demonstrate its utility through applications to simulated and experimentally recorded data from the mouse auditory cortex. eLife Sciences Publications, Ltd 2021-06-28 /pmc/articles/PMC8354639/ /pubmed/34180397 http://dx.doi.org/10.7554/eLife.68046 Text en © 2021, Rupasinghe et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Neuroscience Rupasinghe, Anuththara Francis, Nikolas Liu, Ji Bowen, Zac Kanold, Patrick O Babadi, Behtash Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title | Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title_full | Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title_fullStr | Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title_full_unstemmed | Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title_short | Direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
title_sort | direct extraction of signal and noise correlations from two-photon calcium imaging of ensemble neuronal activity |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8354639/ https://www.ncbi.nlm.nih.gov/pubmed/34180397 http://dx.doi.org/10.7554/eLife.68046 |
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