Jing Wang

Hao Wang, Jiatai Lin, Danyi Li et al.

Mitosis detection is one of the fundamental tasks in computational pathology, which is extremely challenging due to the heterogeneity of mitotic cell. Most of the current studies solve the heterogeneity in the technical aspect by increasing the model complexity. However, lacking consideration of the biological knowledge and the complex model design may lead to the overfitting problem while limited the generalizability of the detection model. In this paper, we systematically study the morphological appearances in different mitotic phases as well as the ambiguous non-mitotic cells and identify that balancing the data and feature diversity can achieve better generalizability. Based on this observation, we propose a novel generalizable framework (MitDet) for mitosis detection. The data diversity is considered by the proposed diversity-guided sample balancing (DGSB). And the feature diversity is preserved by inter- and intra- class feature diversity-preserved module (InCDP). Stain enhancement (SE) module is introduced to enhance the domain-relevant diversity of both data and features simultaneously. Extensive experiments have demonstrated that our proposed model outperforms all the SOTA approaches in several popular mitosis detection datasets in both internal and external test sets using minimal annotation efforts with point annotations only. Comprehensive ablation studies have also proven the effectiveness of the rethinking of data and feature diversity balancing. By analyzing the results quantitatively and qualitatively, we believe that our proposed model not only achieves SOTA performance but also might inspire the future studies in new perspectives. Source code is at https://github.com/Onehour0108/MitDet.

Andrew Moyes, Richard Gault, Kun Zhang et al.

Domain shift is a problem commonly encountered when developing automated histopathology pipelines. The performance of machine learning models such as convolutional neural networks within automated histopathology pipelines is often diminished when applying them to novel data domains due to factors arising from differing staining and scanning protocols. The Dual-Channel Auto-Encoder (DCAE) model was previously shown to produce feature representations that are less sensitive to appearance variation introduced by different digital slide scanners. In this work, the Multi-Channel Auto-Encoder (MCAE) model is presented as an extension to DCAE which learns from more than two domains of data. Additionally, a synthetic dataset is generated using CycleGANs that contains aligned tissue images that have had their appearance synthetically modified. Experimental results show that the MCAE model produces feature representations that are less sensitive to inter-domain variations than the comparative StaNoSA method when tested on the novel synthetic data. Additionally, the MCAE and StaNoSA models are tested on a novel tissue classification task. The results of this experiment show the MCAE model out performs the StaNoSA model by 5 percentage-points in the f1-score. These results show that the MCAE model is able to generalise better to novel data and tasks than existing approaches by actively learning normalised feature representations.