Evidence map›Paper›PMID 41592127›Full record

ArticlePLoS biology2026

A deep learning-based computational pipeline predicts developmental outcome in retinal organoids.

Cassian Afting, Norin Bhatti, Christina Schlagheck, Encarnación Sánchez Salvador, Laura Herrera-Astorga, Rashi Agarwal, Risa Suzuki, Nicolaj Hackert, Hanns-Martin Lorenz, Lucie Zilova and 2 more

Abstract read
In one paragraph

Article in PLoS biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
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.

Cassian AftingCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Norin BhattiCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Christina SchlagheckCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Encarnación Sánchez SalvadorCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Laura Herrera-AstorgaCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Rashi AgarwalCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Risa SuzukiCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Nicolaj HackertDivision of Rheumatology, Department of Medicine V, Heidelberg University Hospital, Heidelberg, Germany.
Hanns-Martin LorenzDivision of Rheumatology, Department of Medicine V, Heidelberg University Hospital, Heidelberg, Germany.
Lucie ZilovaCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.
Joachim WittbrodtCentre for Organismal Studies Heidelberg (COS), Heidelberg University, Heidelberg, Germany.ORCID 0000-0001-8550-7377
Tarik ExnerHeidelberg International Biosciences Graduate School HBIGS, Heidelberg, Germany.ORCID 0000-0002-3131-2133

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Retinal organoids have become important models for studying development and disease, yet stochastic heterogeneity in the formation of cell types, tissues, and phenotypes remains a major challenge. This limits our ability to precisely experimentally address the early developmental trajectories towards these outcomes. Here, we utilize deep learning to predict the differentiation path and resulting tissues in retinal organoids well before they become visually discernible. Our approach effectively bypasses the challenge of organoid-related heterogeneity in tissue formation. For this, we acquired a high-resolution time-lapse imaging dataset comprising about 1,000 organoids and over 100,000 images enabling precise temporal tracking of organoid development. By combining expert annotations with advanced image analysis of organoid morphology, we characterized the heterogeneity of the retinal pigmented epithelium (RPE) and lens tissues, as well as global organoid morphologies over time. Using this training set, our deep learning approach accurately predicts the emergence and size of RPE and lens tissue formation as well as similarities in overall organoid morphology on an organoid-by-organoid basis at early developmental stages, refining our understanding of when early lineage decisions are made. This approach advances knowledge of tissue and phenotype decision-making in organoid development and can inform the design of similar predictive platforms for other organoid systems, paving the way for more standardized and reproducible organoid research. Finally, it provides a direct focus on early developmental time points for in-depth molecular analyses, alleviated from confounding effects of heterogeneity.

Indexed as

Deep LearningOrganoidsRetinaAnimalsCell DifferentiationHumansImage Processing, Computer-AssistedLens, CrystallinePredictive Learning ModelsRetinal Pigment EpitheliumTime-Lapse Imaging

Identifiers

PMID41592127
PMCPMC12843511

What Socratic holds

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LicenceCC BY
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Registered trials

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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.