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ERCPMP-Gx: Endoscopic Image and Video Dataset for Morphological, Histopathological, and Genomic Characterization of Colorectal Polyposis

Research Medical/Healthcare AI

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Representative image for ERCPMP-Gx: Endoscopic Image and Video Dataset for Morphological, Histopathological, and Genomic Characterization of Colorectal Polyposis

Merged summary

TL;DR - ERCPMP-Gx is a public, patient-level dataset linking colorectal polyposis endoscopy images and videos with histopathology and germline findings. It addresses a gap in multimodal data for AI-assisted recognition and classification of hereditary polyposis syndromes.

  • Contains 160 images plus video clips captured with white-light and multiple narrow-band imaging modes.
  • Approximately 80% of cases involve clinically or genetically confirmed hereditary syndromes; 20% are non-hereditary polyps or mimicking lesions for differential classification.
  • Covers familial adenomatous, Peutz-Jeghers, juvenile, and ganglioneuroma polyposis syndromes.
  • Records include standardized endoscopic annotations and, where available, representative histopathology and clinically reported germline findings.

Sources (1)

ERCPMP-Gx: Endoscopic Image and Video Dataset for Morphological, Histopathological, and Genomic Characterization of Colorectal Polyposis

arXiv cs.CV Zahra Ghaffari, Massih Bahar, Mojgan Forootan, Ali Darvishi, Hamidreza Bolhasani 2026-09-17 arXiv:2609.20815 doi:10.17632/nzyfc544bx.2)
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Providers: Hugging Face · N/A OpenAlex · N/A Publisher · N/A Semantic Scholar · N/A X · N/A Fetched 2026-09-26 14:15:29.553326 UTC

TL;DR - ERCPMP-Gx is a public, patient-level dataset linking colorectal polyposis endoscopy images and videos with histopathology and germline findings. It addresses a gap in multimodal data for AI-assisted recognition and classification of hereditary polyposis syndromes.

  • Contains 160 images plus video clips captured with white-light and multiple narrow-band imaging modes.
  • Approximately 80% of cases involve clinically or genetically confirmed hereditary syndromes; 20% are non-hereditary polyps or mimicking lesions for differential classification.
  • Covers familial adenomatous, Peutz-Jeghers, juvenile, and ganglioneuroma polyposis syndromes.
  • Records include standardized endoscopic annotations and, where available, representative histopathology and clinically reported germline findings.
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