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Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data

Widefield microscopy can provide optical access to multi-millimeter fields of view and thousands of neurons in mammalian brains at video rate. However, tissue scattering and background contamination results in signal deterioration, making the extraction of neuronal activity challenging, laborious an...

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Autores principales: Zhang, Yuanlong, Zhang, Guoxun, Han, Xiaofei, Wu, Jiamin, Li, Ziwei, Li, Xinyang, Xiao, Guihua, Xie, Hao, Fang, Lu, Dai, Qionghai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172132/
https://www.ncbi.nlm.nih.gov/pubmed/37002377
http://dx.doi.org/10.1038/s41592-023-01838-7
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author Zhang, Yuanlong
Zhang, Guoxun
Han, Xiaofei
Wu, Jiamin
Li, Ziwei
Li, Xinyang
Xiao, Guihua
Xie, Hao
Fang, Lu
Dai, Qionghai
author_facet Zhang, Yuanlong
Zhang, Guoxun
Han, Xiaofei
Wu, Jiamin
Li, Ziwei
Li, Xinyang
Xiao, Guihua
Xie, Hao
Fang, Lu
Dai, Qionghai
author_sort Zhang, Yuanlong
collection PubMed
description Widefield microscopy can provide optical access to multi-millimeter fields of view and thousands of neurons in mammalian brains at video rate. However, tissue scattering and background contamination results in signal deterioration, making the extraction of neuronal activity challenging, laborious and time consuming. Here we present our deep-learning-based widefield neuron finder (DeepWonder), which is trained by simulated functional recordings and effectively works on experimental data to achieve high-fidelity neuronal extraction. Equipped with systematic background contribution priors, DeepWonder conducts neuronal inference with an order-of-magnitude-faster speed and improved accuracy compared with alternative approaches. DeepWonder removes background contaminations and is computationally efficient. Specifically, DeepWonder accomplishes 50-fold signal-to-background ratio enhancement when processing terabytes-scale cortex-wide functional recordings, with over 14,000 neurons extracted in 17 h.
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spelling pubmed-101721322023-05-12 Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data Zhang, Yuanlong Zhang, Guoxun Han, Xiaofei Wu, Jiamin Li, Ziwei Li, Xinyang Xiao, Guihua Xie, Hao Fang, Lu Dai, Qionghai Nat Methods Article Widefield microscopy can provide optical access to multi-millimeter fields of view and thousands of neurons in mammalian brains at video rate. However, tissue scattering and background contamination results in signal deterioration, making the extraction of neuronal activity challenging, laborious and time consuming. Here we present our deep-learning-based widefield neuron finder (DeepWonder), which is trained by simulated functional recordings and effectively works on experimental data to achieve high-fidelity neuronal extraction. Equipped with systematic background contribution priors, DeepWonder conducts neuronal inference with an order-of-magnitude-faster speed and improved accuracy compared with alternative approaches. DeepWonder removes background contaminations and is computationally efficient. Specifically, DeepWonder accomplishes 50-fold signal-to-background ratio enhancement when processing terabytes-scale cortex-wide functional recordings, with over 14,000 neurons extracted in 17 h. Nature Publishing Group US 2023-04-01 2023 /pmc/articles/PMC10172132/ /pubmed/37002377 http://dx.doi.org/10.1038/s41592-023-01838-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Zhang, Yuanlong
Zhang, Guoxun
Han, Xiaofei
Wu, Jiamin
Li, Ziwei
Li, Xinyang
Xiao, Guihua
Xie, Hao
Fang, Lu
Dai, Qionghai
Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title_full Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title_fullStr Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title_full_unstemmed Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title_short Rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
title_sort rapid detection of neurons in widefield calcium imaging datasets after training with synthetic data
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10172132/
https://www.ncbi.nlm.nih.gov/pubmed/37002377
http://dx.doi.org/10.1038/s41592-023-01838-7
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