Saved in:
Bibliographic Details
Main Authors: Jiang, Yiyang, Qian, Guangwu, Wu, Jiaxin, Huang, Qi, Li, Qing, Wu, Yongkang, Wei, Xiao-Yong
Format: Preprint
Published: 2025
Subjects:
Online Access:https://arxiv.org/abs/2511.21519
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1866909989715574784
author Jiang, Yiyang
Qian, Guangwu
Wu, Jiaxin
Huang, Qi
Li, Qing
Wu, Yongkang
Wei, Xiao-Yong
author_facet Jiang, Yiyang
Qian, Guangwu
Wu, Jiaxin
Huang, Qi
Li, Qing
Wu, Yongkang
Wei, Xiao-Yong
contents Antinuclear antibody (ANA) testing is a crucial method for diagnosing autoimmune disorders, including lupus, Sjögren's syndrome, and scleroderma. Despite its importance, manual ANA detection is slow, labor-intensive, and demands years of training. ANA detection is complicated by over 100 coexisting antibody types, resulting in vast fluorescent pattern combinations. Although machine learning and deep learning have enabled automation, ANA detection in real-world clinical settings presents unique challenges as it involves multi-instance, multi-label (MIML) learning. In this paper, a novel framework for ANA detection is proposed that handles the complexities of MIML tasks using unaltered microscope images without manual preprocessing. Inspired by human labeling logic, it identifies consistent ANA sub-regions and assigns aggregated labels accordingly. These steps are implemented using three task-specific components: an instance sampler, a probabilistic pseudo-label dispatcher, and self-paced weight learning rate coefficients. The instance sampler suppresses low-confidence instances by modeling pattern confidence, while the dispatcher adaptively assigns labels based on instance distinguishability. Self-paced learning adjusts training according to empirical label observations. Our framework overcomes limitations of traditional MIML methods and supports end-to-end optimization. Extensive experiments on one ANA dataset and three public medical MIML benchmarks demonstrate the superiority of our framework. On the ANA dataset, our model achieves up to +7.0% F1-Macro and +12.6% mAP gains over the best prior method, setting new state-of-the-art results. It also ranks top-2 across all key metrics on public datasets, reducing Hamming loss and one-error by up to 18.2% and 26.9%, respectively. The source code can be accessed at https://github.com/fletcherjiang/ANA-SelfPacedLearning.
format Preprint
id arxiv_https___arxiv_org_abs_2511_21519
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Self-Paced Learning for Images of Antinuclear Antibodies
Jiang, Yiyang
Qian, Guangwu
Wu, Jiaxin
Huang, Qi
Li, Qing
Wu, Yongkang
Wei, Xiao-Yong
Computer Vision and Pattern Recognition
Antinuclear antibody (ANA) testing is a crucial method for diagnosing autoimmune disorders, including lupus, Sjögren's syndrome, and scleroderma. Despite its importance, manual ANA detection is slow, labor-intensive, and demands years of training. ANA detection is complicated by over 100 coexisting antibody types, resulting in vast fluorescent pattern combinations. Although machine learning and deep learning have enabled automation, ANA detection in real-world clinical settings presents unique challenges as it involves multi-instance, multi-label (MIML) learning. In this paper, a novel framework for ANA detection is proposed that handles the complexities of MIML tasks using unaltered microscope images without manual preprocessing. Inspired by human labeling logic, it identifies consistent ANA sub-regions and assigns aggregated labels accordingly. These steps are implemented using three task-specific components: an instance sampler, a probabilistic pseudo-label dispatcher, and self-paced weight learning rate coefficients. The instance sampler suppresses low-confidence instances by modeling pattern confidence, while the dispatcher adaptively assigns labels based on instance distinguishability. Self-paced learning adjusts training according to empirical label observations. Our framework overcomes limitations of traditional MIML methods and supports end-to-end optimization. Extensive experiments on one ANA dataset and three public medical MIML benchmarks demonstrate the superiority of our framework. On the ANA dataset, our model achieves up to +7.0% F1-Macro and +12.6% mAP gains over the best prior method, setting new state-of-the-art results. It also ranks top-2 across all key metrics on public datasets, reducing Hamming loss and one-error by up to 18.2% and 26.9%, respectively. The source code can be accessed at https://github.com/fletcherjiang/ANA-SelfPacedLearning.
title Self-Paced Learning for Images of Antinuclear Antibodies
topic Computer Vision and Pattern Recognition
url https://arxiv.org/abs/2511.21519