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

dc.contributor.authorCapek, Daniel
dc.contributor.authorSafroshkin, Matvey
dc.contributor.authorMorales-Navarrete, Hernán
dc.contributor.authorToulany, Nikan
dc.contributor.authorArutyunov, Grigory
dc.contributor.authorKurzbach, Anica
dc.contributor.authorBihler, Johanna
dc.contributor.authorHagauer, Julia
dc.contributor.authorJordan, Ben
dc.contributor.authorMüller, Patrick
dc.date.accessioned2023-06-05T14:11:31Z
dc.date.available2023-06-05T14:11:31Z
dc.date.issued2023-05-08
dc.description.abstractEvolutionarily 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.
dc.description.versionpublisheddeu
dc.identifier.doi10.1038/s41592-023-01873-4
dc.identifier.ppn1847426999
dc.identifier.urihttps://kops.uni-konstanz.de/handle/123456789/67064
dc.language.isoeng
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.ddc570
dc.titleEmbryoNet : using deep learning to link embryonic phenotypes to signaling pathwayseng
dc.typeJOURNAL_ARTICLE
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  title={EmbryoNet : using deep learning to link embryonic phenotypes to signaling pathways},
  year={2023},
  doi={10.1038/s41592-023-01873-4},
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  journal={Nature Methods},
  pages={815--823},
  author={Capek, Daniel and Safroshkin, Matvey and Morales-Navarrete, Hernán and Toulany, Nikan and Arutyunov, Grigory and Kurzbach, Anica and Bihler, Johanna and Hagauer, Julia and Jordan, Ben and Müller, Patrick}
}
kops.citation.iso690CAPEK, Daniel, Matvey SAFROSHKIN, Hernán MORALES-NAVARRETE, Nikan TOULANY, Grigory ARUTYUNOV, Anica KURZBACH, Johanna BIHLER, Julia HAGAUER, Ben JORDAN, Patrick MÜLLER, 2023. EmbryoNet : using deep learning to link embryonic phenotypes to signaling pathways. In: Nature Methods. Springer. 2023, 20, S. 815-823. ISSN 1548-7091. eISSN 1548-7105. Verfügbar unter: doi: 10.1038/s41592-023-01873-4deu
kops.citation.iso690CAPEK, Daniel, Matvey SAFROSHKIN, Hernán MORALES-NAVARRETE, Nikan TOULANY, Grigory ARUTYUNOV, Anica KURZBACH, Johanna BIHLER, Julia HAGAUER, Ben JORDAN, Patrick MÜLLER, 2023. EmbryoNet : using deep learning to link embryonic phenotypes to signaling pathways. In: Nature Methods. Springer. 2023, 20, pp. 815-823. ISSN 1548-7091. eISSN 1548-7105. Available under: doi: 10.1038/s41592-023-01873-4eng
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