Evidence map›Paper›PMID 37156842›Full record

ArticleNature methods2023

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

Daniel Čapek, Matvey Safroshkin, Hernán Morales-Navarrete, Nikan Toulany, Grigory Arutyunov, Anica Kurzbach, Johanna Bihler, Julia Hagauer, Sebastian Kick, Felicity Jones and 2 more

Abstract read
In one paragraph

Article in Nature methods, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed.

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  5. A quantitative coordinate system for developmental dynamics.bioRxiv : the preprint server for biology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Daniel Čapek *Systems Biology of Development, University of Konstanz, Konstanz, Germany.ORCID 0000-0001-5199-9940
Matvey Safroshkin *Computer Vision Studio, Tübingen, Germany.
Hernán Morales-Navarrete *Systems Biology of Development, University of Konstanz, Konstanz, Germany.ORCID 0000-0002-9578-2556
Nikan ToulanySystems Biology of Development, University of Konstanz, Konstanz, Germany.ORCID 0000-0003-3505-7325
Grigory ArutyunovComputer Vision Studio, Tübingen, Germany.
Anica KurzbachSystems Biology of Development, University of Konstanz, Konstanz, Germany.
Johanna BihlerFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Julia HagauerFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Sebastian KickFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Felicity JonesFriedrich Miescher Laboratory of the Max Planck Society, Tübingen, Germany.
Ben JordanSystems Biology of Development, University of Konstanz, Konstanz, Germany.
Patrick MüllerSystems Biology of Development, University of Konstanz, Konstanz, Germany. patrick.mueller@uni-konstanz.de.ORCID 0000-0002-0702-6209

Funding

Austrian Science Fund (Fonds zur Förderung der Wissenschaftlichen Forschung) J-4507Austrian Science Fund FWF J 4507Deutsche Forschungsgemeinschaft (German Research Foundation) EXC 2117 - 422037984EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) 863952
6 · The paper itself

Abstract

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.

Indexed as

Deep LearningAlgorithmsAnimalsNeural Networks, ComputerPhenotypeSignal TransductionZebrafish

Identifiers

PMID37156842
PMCPMC10250202

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.