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EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways

Evolutionarily conserved signaling pathways are essential for early embryogenesis, and reducing or abolishing their activity leads to characteristic developmental defects. Classification of phenotypic defects can identify the underlying signaling mechanisms, but this requires expert knowledge and th...

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Autores principales: Čapek, Daniel, Safroshkin, Matvey, Morales-Navarrete, Hernán, Toulany, Nikan, Arutyunov, Grigory, Kurzbach, Anica, Bihler, Johanna, Hagauer, Julia, Kick, Sebastian, Jones, Felicity, Jordan, Ben, Müller, Patrick
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250202/
https://www.ncbi.nlm.nih.gov/pubmed/37156842
http://dx.doi.org/10.1038/s41592-023-01873-4
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author Čapek, Daniel
Safroshkin, Matvey
Morales-Navarrete, Hernán
Toulany, Nikan
Arutyunov, Grigory
Kurzbach, Anica
Bihler, Johanna
Hagauer, Julia
Kick, Sebastian
Jones, Felicity
Jordan, Ben
Müller, Patrick
author_facet Čapek, Daniel
Safroshkin, Matvey
Morales-Navarrete, Hernán
Toulany, Nikan
Arutyunov, Grigory
Kurzbach, Anica
Bihler, Johanna
Hagauer, Julia
Kick, Sebastian
Jones, Felicity
Jordan, Ben
Müller, Patrick
author_sort Čapek, Daniel
collection PubMed
description Evolutionarily conserved signaling pathways are essential for early embryogenesis, and reducing or abolishing their activity leads to characteristic developmental defects. Classification of phenotypic defects can identify the underlying signaling mechanisms, but this requires expert knowledge and the classification schemes have not been standardized. Here we use a machine learning approach for automated phenotyping to train a deep convolutional neural network, EmbryoNet, to accurately identify zebrafish signaling mutants in an unbiased manner. Combined with a model of time-dependent developmental trajectories, this approach identifies and classifies with high precision phenotypic defects caused by loss of function of the seven major signaling pathways relevant for vertebrate development. Our classification algorithms have wide applications in developmental biology and robustly identify signaling defects in evolutionarily distant species. Furthermore, using automated phenotyping in high-throughput drug screens, we show that EmbryoNet can resolve the mechanism of action of pharmaceutical substances. As part of this work, we freely provide more than 2 million images that were used to train and test EmbryoNet.
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spelling pubmed-102502022023-06-10 EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways Čapek, Daniel Safroshkin, Matvey Morales-Navarrete, Hernán Toulany, Nikan Arutyunov, Grigory Kurzbach, Anica Bihler, Johanna Hagauer, Julia Kick, Sebastian Jones, Felicity Jordan, Ben Müller, Patrick Nat Methods Resource Evolutionarily conserved signaling pathways are essential for early embryogenesis, and reducing or abolishing their activity leads to characteristic developmental defects. Classification of phenotypic defects can identify the underlying signaling mechanisms, but this requires expert knowledge and the classification schemes have not been standardized. Here we use a machine learning approach for automated phenotyping to train a deep convolutional neural network, EmbryoNet, to accurately identify zebrafish signaling mutants in an unbiased manner. Combined with a model of time-dependent developmental trajectories, this approach identifies and classifies with high precision phenotypic defects caused by loss of function of the seven major signaling pathways relevant for vertebrate development. Our classification algorithms have wide applications in developmental biology and robustly identify signaling defects in evolutionarily distant species. Furthermore, using automated phenotyping in high-throughput drug screens, we show that EmbryoNet can resolve the mechanism of action of pharmaceutical substances. As part of this work, we freely provide more than 2 million images that were used to train and test EmbryoNet. Nature Publishing Group US 2023-05-08 2023 /pmc/articles/PMC10250202/ /pubmed/37156842 http://dx.doi.org/10.1038/s41592-023-01873-4 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 Resource
Čapek, Daniel
Safroshkin, Matvey
Morales-Navarrete, Hernán
Toulany, Nikan
Arutyunov, Grigory
Kurzbach, Anica
Bihler, Johanna
Hagauer, Julia
Kick, Sebastian
Jones, Felicity
Jordan, Ben
Müller, Patrick
EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title_full EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title_fullStr EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title_full_unstemmed EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title_short EmbryoNet: using deep learning to link embryonic phenotypes to signaling pathways
title_sort embryonet: using deep learning to link embryonic phenotypes to signaling pathways
topic Resource
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10250202/
https://www.ncbi.nlm.nih.gov/pubmed/37156842
http://dx.doi.org/10.1038/s41592-023-01873-4
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