ArticleMolecular systems biology2024
PIFiA: self-supervised approach for protein functional annotation from single-cell imaging data.
Article in Molecular systems biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed.
- Progress and new challenges in image-based profiling.Molecular systems biology · 2026Review
- A comprehensive overview of yeast libraries and their role in advancing cell biology.The FEBS journal · 2026Review
- Cell context-dependent in silico organelle localization in label-free microscopy images.Nature methods · 2026Article
- Article
- Capturing cell heterogeneity in representations of cell populations for image-based profiling using contrastive learning.PLoS computational biology · 2024Article
- Visual interpretability of bioimaging deep learning models.Nature methods · 2024Article
- Capturing cell heterogeneity in representations of cell populations for image-based profiling using contrastive learning.bioRxiv : the preprint server for biology · 2024Article
- Expanding TheCellVision.org: a central repository for visualizing and mining high-content cell imaging projects.Genetics · 2024Article
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10 authors.
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Abstract
Fluorescence microscopy data describe protein localization patterns at single-cell resolution and have the potential to reveal whole-proteome functional information with remarkable precision. Yet, extracting biologically meaningful representations from cell micrographs remains a major challenge. Existing approaches often fail to learn robust and noise-invariant features or rely on supervised labels for accurate annotations. We developed PIFiA (Protein Image-based Functional Annotation), a self-supervised approach for protein functional annotation from single-cell imaging data. We imaged the global yeast ORF-GFP collection and applied PIFiA to generate protein feature profiles from single-cell images of fluorescently tagged proteins. We show that PIFiA outperforms existing approaches for molecular representation learning and describe a range of downstream analysis tasks to explore the information content of the feature profiles. Specifically, we cluster extracted features into a hierarchy of functional organization, study cell population heterogeneity, and develop techniques to distinguish multi-localizing proteins and identify functional modules. Finally, we confirm new PIFiA predictions using a colocalization assay, suggesting previously unappreciated biological roles for several proteins. Paired with a fully interactive website ( https://thecellvision.org/pifia/ ), PIFiA is a resource for the quantitative analysis of protein organization within the cell.
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