通过形态约束提升疟疾显微图像跨制备方式的泛化能力
MORPHA: Morphology-Constrained Training and the Limits of Cross-Acquisition Transfer in Low-Resource Malaria Microscopy

- 引入形态一致性约束,基于真实标注数据统计寄生虫阶段特征
- 跨制备方式检测性能提升30.8%,校准误差降低49%
- 为低资源场景下的模型设计提供可落地的形态引导策略
在低资源疟疾显微图像分析中,模型在一种涂片制备方式上训练后常需处理另一种制备方式的数据,而形态特征能否有效跨域迁移尚不明确。本文基于乌干达实地采集的真实显微图像(Lacuna数据集),研究将寄生虫形态信息作为训练约束对跨制备迁移的影响。提出MORPHA方法,利用阶段标注的BBBC041数据集提取阶段条件统计量,对偏离该分布的预测施加惩罚,且不改变模型架构与推理流程。该约束在二分类、目标级和阶段感知三种范式中统一适用。在从薄涂片向厚涂片场域图像迁移时,该约束使二分类泛化性能下降减少30.8%(F1从0.578升至0.699),校准误差降低49%(ECE从0.0162降至0.0082)。随机统计对照组仅恢复25.3%的性能损失,说明真实形态内容本身带来增益。两种标准置信度正则化器在原始迁移中表现更优,表明形态约束在特定场景才具价值。进一步揭示两个关键边界:薄涂片统计无法迁移至厚涂片检测(滋养体[email protected]降至0.000),且跨制备伪标签在过滤前即失效。研究结果提供了基于形态的稳定性信号,并为低资源疟疾数据集与模型设计提供实证指导。
原文摘要 · Abstract (English)
In low-resource malaria microscopy, a model trained on one smear preparation routinely meets images from another, and how well morphology-based constraints transfer across this acquisition gap is unclear. We study this on real African field microscopy from Uganda (Lacuna), asking where encoding measured parasite morphology as a training constraint improves cross-acquisition transfer and where generic regularisation suffices. We present MORPHA, a morphological consistency constraint that derives stage-conditional statistics from the stage-annotated BBBC041 dataset and penalises predictions that deviate from them. Defined uniformly across binary, object-level, and stage-aware regimes without changing architecture or inference, it shapes training in the binary regime. The detection regime is a mapped boundary. On transfer from thin-smear cells to thick-smear field images, the constraint reduces the binary-classification generalisation drop by 30.8% (F1 0.578 to 0.699) at negligible within-domain cost and lowers in-distribution calibration error by 49% (ECE 0.0162 to 0.0082). A content-free control applying the identical constraint to random statistics recovers less of the drop (25.3% vs 30.8%), indicating the measured content, not constraining alone, contributes to the gain. Two standard confidence regularisers exceed the constraint on raw transfer, locating where morphology adds value and where generic regularisation suffices. We map two deployment-relevant boundaries: thin-smear statistics do not transfer to thick-smear detection (trophozoite [email protected] falls to 0.000), and cross-acquisition pseudo-labelling fails before filtering applies. Together these yield a morphology-grounded consistency signal and evidence-based guidance for malaria dataset and model design in low-resource settings.
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