ArticleNature communications2025
PHARAOH: A collaborative crowdsourcing platform for phenotyping and regional analysis of histology.
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.
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Who cites it
5 citing papers in PubMed.
- Compositional and interpretable representation of histology using AI foundation models and sparse autoencoders.bioRxiv : the preprint server for biology · 2026Article
- Dysmorphic neurons express markers of inhibitory glycinergic signaling in focal cortical dysplasia IIb.Brain pathology (Zurich, Switzerland) · 2026Article
- Digital Pathology-Based Comparison of PyRadiomics and HistomicsTK for Nuclei Classification in Melanoma Whole Slide Images.International journal of biomedical imaging · 2026Article
- Integrative whole slide image and spatial transcriptomics analysis with QuST and QuPath.NPJ precision oncology · 2025Article
- Fractal dimensions for tumour-related cell types of prostate cancer on histopathology images using multiple-threshold box counting algorithm.Biophysics and physicobiology · 2025Article
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Authors and funding
31 authors.
Funding
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Abstract
Deep learning has proven capable of automating key aspects of histopathologic analysis. However, its context-specific nature and continued reliance on large expert-annotated training datasets hinders the development of a critical mass of applications to garner widespread adoption in clinical/research workflows. Here, we present an online collaborative platform that streamlines tissue image annotation to promote the development and sharing of custom computer vision models for PHenotyping And Regional Analysis Of Histology (PHARAOH; https://www.pathologyreports.ai/ ). Specifically, PHARAOH uses a weakly supervised, human-in-the-loop learning framework whereby patch-level image features are leveraged to organize large swaths of tissue into morphologically-uniform clusters for batched annotation by human experts. By providing cluster-level labels on only a handful of cases, we show how custom PHARAOH models can be developed efficiently and used to guide the quantification of cellular features that correlate with molecular, pathologic and patient outcome data. Moreover, by using our PHARAOH pipeline, we showcase how correlation of cohort-level cytoarchitectural features with accompanying biological and outcome data can help systematically devise interpretable morphometric models of disease. Both the custom model design and feature extraction pipelines are amenable to crowdsourcing, positioning PHARAOH to become a fully scalable, systems-level solution for the expansion, generalization and cataloging of computational pathology applications.
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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.