ArticleNature communications2025
Generalizable morphological profiling of cells by interpretable unsupervised learning.
Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
What it found
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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.
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.
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Who cites it
5 citing papers in PubMed.
- Overview of State-of-the-Art Learning-Based Classification Methods in Medical Imaging.Annals of biomedical engineering · 2026Review
- Progress and new challenges in image-based profiling.Molecular systems biology · 2026Review
- Review
- Generalizable morphological profiling of cells by interpretable unsupervised learning.Nature communications · 2025Article
- Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
The intersection of advanced microscopy and machine learning is transforming cell biology into a quantitative, data-driven field. Traditional cell profiling depends on manual feature extraction, which is labor-intensive and prone to bias, while deep learning provides alternatives but faces challenges with interpretability and reliance on labeled data. We present MorphoGenie, an unsupervised deep-learning framework for single-cell morphological profiling. By combining disentangled representation learning with high-fidelity image reconstruction, MorphoGenie creates a compact, interpretable latent space that captures biologically meaningful features without annotation, overcoming the "curse of dimensionality." Unlike previous models, it systematically links latent representations to hierarchical morphological attributes, ensuring semantic and biological interpretability. It also supports combinatorial generalization, enabling robust performance across diverse imaging modalities (e.g., fluorescence, quantitative phase imaging) and experimental conditions, from discrete cell type/state classification to continuous trajectory inference. This provides a generalized, unbiased strategy for morphological profiling, revealing cellular behaviors often overlooked by expert visual examination.
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Registered trials
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 OpenQuestion graph.