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Superhuman cell death detection with biomarker-optimized neural networks
Cellular events underlying neurodegenerative disease may be captured by longitudinal live microscopy of neurons. While the advent of robot-assisted microscopy has helped scale such efforts to high-throughput regimes with the statistical power to detect transient events, time-intensive human annotati...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654296/ https://www.ncbi.nlm.nih.gov/pubmed/34878844 http://dx.doi.org/10.1126/sciadv.abf8142 |
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author | Linsley, Jeremy W. Linsley, Drew A. Lamstein, Josh Ryan, Gennadi Shah, Kevan Castello, Nicholas A. Oza, Viral Kalra, Jaslin Wang, Shijie Tokuno, Zachary Javaherian, Ashkan Serre, Thomas Finkbeiner, Steven |
author_facet | Linsley, Jeremy W. Linsley, Drew A. Lamstein, Josh Ryan, Gennadi Shah, Kevan Castello, Nicholas A. Oza, Viral Kalra, Jaslin Wang, Shijie Tokuno, Zachary Javaherian, Ashkan Serre, Thomas Finkbeiner, Steven |
author_sort | Linsley, Jeremy W. |
collection | PubMed |
description | Cellular events underlying neurodegenerative disease may be captured by longitudinal live microscopy of neurons. While the advent of robot-assisted microscopy has helped scale such efforts to high-throughput regimes with the statistical power to detect transient events, time-intensive human annotation is required. We addressed this fundamental limitation with biomarker-optimized convolutional neural networks (BO-CNNs): interpretable computer vision models trained directly on biosensor activity. We demonstrate the ability of BO-CNNs to detect cell death, which is typically measured by trained annotators. BO-CNNs detected cell death with superhuman accuracy and speed by learning to identify subcellular morphology associated with cell vitality, despite receiving no explicit supervision to rely on these features. These models also revealed an intranuclear morphology signal that is difficult to spot by eye and had not previously been linked to cell death, but that reliably indicates death. BO-CNNs are broadly useful for analyzing live microscopy and essential for interpreting high-throughput experiments. |
format | Online Article Text |
id | pubmed-8654296 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-86542962021-12-16 Superhuman cell death detection with biomarker-optimized neural networks Linsley, Jeremy W. Linsley, Drew A. Lamstein, Josh Ryan, Gennadi Shah, Kevan Castello, Nicholas A. Oza, Viral Kalra, Jaslin Wang, Shijie Tokuno, Zachary Javaherian, Ashkan Serre, Thomas Finkbeiner, Steven Sci Adv Neuroscience Cellular events underlying neurodegenerative disease may be captured by longitudinal live microscopy of neurons. While the advent of robot-assisted microscopy has helped scale such efforts to high-throughput regimes with the statistical power to detect transient events, time-intensive human annotation is required. We addressed this fundamental limitation with biomarker-optimized convolutional neural networks (BO-CNNs): interpretable computer vision models trained directly on biosensor activity. We demonstrate the ability of BO-CNNs to detect cell death, which is typically measured by trained annotators. BO-CNNs detected cell death with superhuman accuracy and speed by learning to identify subcellular morphology associated with cell vitality, despite receiving no explicit supervision to rely on these features. These models also revealed an intranuclear morphology signal that is difficult to spot by eye and had not previously been linked to cell death, but that reliably indicates death. BO-CNNs are broadly useful for analyzing live microscopy and essential for interpreting high-throughput experiments. American Association for the Advancement of Science 2021-12-08 /pmc/articles/PMC8654296/ /pubmed/34878844 http://dx.doi.org/10.1126/sciadv.abf8142 Text en Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Neuroscience Linsley, Jeremy W. Linsley, Drew A. Lamstein, Josh Ryan, Gennadi Shah, Kevan Castello, Nicholas A. Oza, Viral Kalra, Jaslin Wang, Shijie Tokuno, Zachary Javaherian, Ashkan Serre, Thomas Finkbeiner, Steven Superhuman cell death detection with biomarker-optimized neural networks |
title | Superhuman cell death detection with biomarker-optimized neural networks |
title_full | Superhuman cell death detection with biomarker-optimized neural networks |
title_fullStr | Superhuman cell death detection with biomarker-optimized neural networks |
title_full_unstemmed | Superhuman cell death detection with biomarker-optimized neural networks |
title_short | Superhuman cell death detection with biomarker-optimized neural networks |
title_sort | superhuman cell death detection with biomarker-optimized neural networks |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654296/ https://www.ncbi.nlm.nih.gov/pubmed/34878844 http://dx.doi.org/10.1126/sciadv.abf8142 |
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