arXiv:2510.09583cs.CV2025-10被引 2

一模型搞定罕见寄生虫检测,少样本下也能准识别新物种

FSP-DETR: Few-Shot Prototypical Parasitic Ova Detection

  • 用支持图像构建类别原型,通过增强视图和轻量解码器学特征空间
  • 在20类卵虫数据集上,少样本和开放集检测性能显著优于现有方法
  • 无需重训即可识别未知类别、拒识背景,适合医疗场景的持续学习

生物医学中的目标检测受限于标注数据稀缺及新/罕见类别的频繁出现。本文提出FSP-DETR,一种统一检测框架,可在单一模型中实现鲁棒的少样本检测、开放集识别及未见生物任务的泛化能力。基于类无关的DETR主干,该方法从原始支持图像构建类别原型,并利用增强视图与轻量Transformer解码器学习嵌入空间。联合训练优化原型匹配损失、基于对齐的分离损失及KL散度正则化,以提升稀疏监督下的判别性特征学习与校准能力。不同于以往孤立处理各项任务的方法,FSP-DETR在推理时具备灵活性,支持未见类别识别、背景拒识与跨任务适应而无需重训。我们还引入一个新的卵虫物种检测基准,包含20类寄生虫,并建立标准化评估协议。在卵虫、血细胞及疟疾检测任务上的大量实验表明,FSP-DETR显著优于现有少样本与原型基检测器,尤其在低样本与开放集场景表现突出。

原文摘要 · Abstract (English)

Object detection in biomedical settings is fundamentally constrained by the scarcity of labeled data and the frequent emergence of novel or rare categories. We present FSP-DETR, a unified detection framework that enables robust few-shot detection, open-set recognition, and generalization to unseen biomedical tasks within a single model. Built upon a class-agnostic DETR backbone, our approach constructs class prototypes from original support images and learns an embedding space using augmented views and a lightweight transformer decoder. Training jointly optimizes a prototype matching loss, an alignment-based separation loss, and a KL divergence regularization to improve discriminative feature learning and calibration under scarce supervision. Unlike prior work that tackles these tasks in isolation, FSP-DETR enables inference-time flexibility to support unseen class recognition, background rejection, and cross-task adaptation without retraining. We also introduce a new ova species detection benchmark with 20 parasite classes and establish standardized evaluation protocols. Extensive experiments across ova, blood cell, and malaria detection tasks demonstrate that FSP-DETR significantly outperforms prior few-shot and prototype-based detectors, especially in low-shot and open-set scenarios.

少样本检测生物医学开放集识别原型学习

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