Deep learning is widely applicable to phenotyping embryonic development and disease

Abstract: Genome editing simplifies the generation of new animal models for congenital disorders. However, the detailed and unbiased phenotypic assessment of altered embryonic development remains a challenge. Here, we explore how deep learning (U-Net) can automate segmentation tasks in various imaging modalities, and we quantify phenotypes of altered renal, neural and craniofacial development in Xenopus embryos in comparison with normal variability. We demonstrate the utility of this approach in embryos with polycystic kidneys (pkd1 and pkd2) and craniofacial dysmorphia (six1). We highlight how in toto light-sheet microscopy facilitates accurate reconstruction of brain and craniofacial structures within X. tropicalis embryos upon dyrk1a and six1 loss of function or treatment with retinoic acid inhibitors. These tools increase the sensitivity and throughput of evaluating developmental malformations caused by chemical or genetic disruption. Furthermore, we provide a library of pre-trained networks and detailed instructions for applying deep learning to the reader's own datasets. We demonstrate the versatility, precision and scalability of deep neural network phenotyping on embryonic disease models. By combining light-sheet microscopy and deep learning, we provide a framework for higher-throughput characterization of embryonic model organisms

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch
Notes
Development. - 148, 21 (2021) , dev199664, ISSN: 1477-9129

Event
Veröffentlichung
(where)
Freiburg
(who)
Universität
(when)
2024
Creator
Naert, Thomas
Çiçek, Özgün
Ogar, Paulina
Bürgi, Max
Shaidani, Nikko-Ideen
Kaminski, Michael
Xu, Yuxiao
Grand, Kelli
Vujanovic, Marko
Prata, Daniel
Hildebrandt, Friedhelm
Brox, Thomas
Ronneberger, Olaf
Voigt, Fabian F.
Helmchen, Fritjof
Loffing, Johannes
Horb, Marko E.
Willsey, Helen Rankin
Lienkamp, Soeren

DOI
10.1242/dev.199664
URN
urn:nbn:de:bsz:25-freidok-2481234
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
25.03.2025, 1:46 PM CET

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Associated

Time of origin

  • 2024

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