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New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning
Cellular imaging instrumentation advancements as well as readily available optogenetic and fluorescence sensors have yielded a profound need for fast, accurate, and standardized analysis. Deep-learning architectures have revolutionized the field of biomedical image analysis and have achieved state-o...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095751/ https://www.ncbi.nlm.nih.gov/pubmed/35573197 http://dx.doi.org/10.1016/j.isci.2022.104277 |
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author | Kamran, Sharif Amit Hossain, Khondker Fariha Moghnieh, Hussein Riar, Sarah Bartlett, Allison Tavakkoli, Alireza Sanders, Kenton M. Baker, Salah A. |
author_facet | Kamran, Sharif Amit Hossain, Khondker Fariha Moghnieh, Hussein Riar, Sarah Bartlett, Allison Tavakkoli, Alireza Sanders, Kenton M. Baker, Salah A. |
author_sort | Kamran, Sharif Amit |
collection | PubMed |
description | Cellular imaging instrumentation advancements as well as readily available optogenetic and fluorescence sensors have yielded a profound need for fast, accurate, and standardized analysis. Deep-learning architectures have revolutionized the field of biomedical image analysis and have achieved state-of-the-art accuracy. Despite these advancements, deep learning architectures for the segmentation of subcellular fluorescence signals is lacking. Cellular dynamic fluorescence signals can be plotted and visualized using spatiotemporal maps (STMaps), and currently their segmentation and quantification are hindered by slow workflow speed and lack of accuracy, especially for large datasets. In this study, we provide a software tool that utilizes a deep-learning methodology to fundamentally overcome signal segmentation challenges. The software framework demonstrates highly optimized and accurate calcium signal segmentation and provides a fast analysis pipeline that can accommodate different patterns of signals across multiple cell types. The software allows seamless data accessibility, quantification, and graphical visualization and enables large dataset analysis throughput. |
format | Online Article Text |
id | pubmed-9095751 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-90957512022-05-13 New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning Kamran, Sharif Amit Hossain, Khondker Fariha Moghnieh, Hussein Riar, Sarah Bartlett, Allison Tavakkoli, Alireza Sanders, Kenton M. Baker, Salah A. iScience Article Cellular imaging instrumentation advancements as well as readily available optogenetic and fluorescence sensors have yielded a profound need for fast, accurate, and standardized analysis. Deep-learning architectures have revolutionized the field of biomedical image analysis and have achieved state-of-the-art accuracy. Despite these advancements, deep learning architectures for the segmentation of subcellular fluorescence signals is lacking. Cellular dynamic fluorescence signals can be plotted and visualized using spatiotemporal maps (STMaps), and currently their segmentation and quantification are hindered by slow workflow speed and lack of accuracy, especially for large datasets. In this study, we provide a software tool that utilizes a deep-learning methodology to fundamentally overcome signal segmentation challenges. The software framework demonstrates highly optimized and accurate calcium signal segmentation and provides a fast analysis pipeline that can accommodate different patterns of signals across multiple cell types. The software allows seamless data accessibility, quantification, and graphical visualization and enables large dataset analysis throughput. Elsevier 2022-04-21 /pmc/articles/PMC9095751/ /pubmed/35573197 http://dx.doi.org/10.1016/j.isci.2022.104277 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Kamran, Sharif Amit Hossain, Khondker Fariha Moghnieh, Hussein Riar, Sarah Bartlett, Allison Tavakkoli, Alireza Sanders, Kenton M. Baker, Salah A. New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title | New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title_full | New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title_fullStr | New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title_full_unstemmed | New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title_short | New open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
title_sort | new open-source software for subcellular segmentation and analysis of spatiotemporal fluorescence signals using deep learning |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9095751/ https://www.ncbi.nlm.nih.gov/pubmed/35573197 http://dx.doi.org/10.1016/j.isci.2022.104277 |
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