用伪标签解混和合成增强提升重叠类器官分割精度
Boosting Overlapping Organoid Instance Segmentation Using Pseudo-Label Unmixing and Synthesis-Assisted Learning
- 通过伪标签解混识别并修正重叠区域的错误标注
- 仅用10%标注数据即达全监督模型性能,超越现有方法
- 适合需要少标注数据的类器官高通量分析场景
类器官是模拟人体组织功能和药物反应的重要体外模型,其精准实例分割对动态行为量化至关重要,但受限于高质量标注数据稀缺及显微图像中普遍存在的重叠问题。尽管半监督学习(SSL)可缓解标注依赖,传统框架因噪声伪标签产生偏差,尤其在重叠区域表现不佳。本文首次将合成辅助半监督学习(SA-SSL)应用于类器官实例分割,发现其仍难以区分纠缠的类器官,常将其误判为单一实体。为此提出伪标签解混(PLU),识别重叠区域错误伪标签并基于实例分解重构标签;采用基于轮廓的合成方法高效生成重叠类器官图像;在图像合成前对伪标签实施实例级增强(IA),进一步提升合成数据效果。在两个类器官数据集上的实验表明,本方法仅用10%标注数据即达到全监督模型水平,实现当前最优性能。消融实验验证了PLU、轮廓合成与增强感知训练的有效性。通过在伪标签与合成层面协同解决重叠问题,推动了可扩展、低标注依赖的类器官分析,为精准医学高通量应用开辟新路径。
原文摘要 · Abstract (English)
Organoids, sophisticated in vitro models of human tissues, are crucial for medical research due to their ability to simulate organ functions and assess drug responses accurately. Accurate organoid instance segmentation is critical for quantifying their dynamic behaviors, yet remains profoundly limited by high-quality annotated datasets and pervasive overlap in microscopy imaging. While semi-supervised learning (SSL) offers a solution to alleviate reliance on scarce labeled data, conventional SSL frameworks suffer from biases induced by noisy pseudo-labels, particularly in overlapping regions. Synthesis-assisted SSL (SA-SSL) has been proposed for mitigating training biases in semi-supervised semantic segmentation. We present the first adaptation of SA-SSL to organoid instance segmentation and reveal that SA-SSL struggles to disentangle intertwined organoids, often misrepresenting overlapping instances as a single entity. To overcome this, we propose Pseudo-Label Unmixing (PLU), which identifies erroneous pseudo-labels for overlapping instances and then regenerates organoid labels through instance decomposition. For image synthesis, we apply a contour-based approach to synthesize organoid instances efficiently, particularly for overlapping cases. Instance-level augmentations (IA) on pseudo-labels before image synthesis further enhances the effect of synthetic data (SD). Rigorous experiments on two organoid datasets demonstrate our method's effectiveness, achieving performance comparable to fully supervised models using only 10% labeled data, and state-of-the-art results. Ablation studies validate the contributions of PLU, contour-based synthesis, and augmentation-aware training. By addressing overlap at both pseudo-label and synthesis levels, our work advances scalable, label-efficient organoid analysis, unlocking new potential for high-throughput applications in precision medicine.
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