ArticleDiagnostics (Basel, Switzerland)2023
Deep Active Learning for Automatic Mitotic Cell Detection on HEp-2 Specimen Medical Images.
Article in Diagnostics (Basel, Switzerland), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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7 citing papers in PubMed.
- Phenotypic switching of gastrointestinal smooth muscle cells and the regulatory role of macrophages: a literature review.Inflammation research : official journal of the European Histamine Research Society ... [et al.] · 2026Review
- Detection of Auto-Immune Disease using Deep Learning Techniques.Mediterranean journal of rheumatology · 2025Article
- Applications, image analysis, and interpretation of computer vision in medical imaging.Frontiers in radiology · 2025Review
- Transferable deep learning with coati optimization algorithm based mitotic nuclei segmentation and classification model.Scientific reports · 2024Article
- Automatic detection and visualization of temporomandibular joint effusion with deep neural network.Scientific reports · 2024Article
- Recognition of rare antinuclear antibody patterns based on a novel attention-based enhancement framework.Briefings in bioinformatics · 2024Article
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6 authors.
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Abstract
Identifying Human Epithelial Type 2 (HEp-2) mitotic cells is a crucial procedure in anti-nuclear antibodies (ANAs) testing, which is the standard protocol for detecting connective tissue diseases (CTD). Due to the low throughput and labor-subjectivity of the ANAs' manual screening test, there is a need to develop a reliable HEp-2 computer-aided diagnosis (CAD) system. The automatic detection of mitotic cells from the microscopic HEp-2 specimen images is an essential step to support the diagnosis process and enhance the throughput of this test. This work proposes a deep active learning (DAL) approach to overcoming the cell labeling challenge. Moreover, deep learning detectors are tailored to automatically identify the mitotic cells directly in the entire microscopic HEp-2 specimen images, avoiding the segmentation step. The proposed framework is validated using the I3A Task-2 dataset over 5-fold cross-validation trials. Using the YOLO predictor, promising mitotic cell prediction results are achieved with an average of 90.011% recall, 88.307% precision, and 81.531% mAP. Whereas, average scores of 86.986% recall, 85.282% precision, and 78.506% mAP are obtained using the Faster R-CNN predictor. Employing the DAL method over four labeling rounds effectively enhances the accuracy of the data annotation, and hence, improves the prediction performance. The proposed framework could be practically applicable to support medical personnel in making rapid and accurate decisions about the mitotic cells' existence.
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