Chunlong Luo

Chunlong Luo, Tianqi Yu, Yufan Luo et al.

Chromosome classification is an important but difficult and tedious task in karyotyping. Previous methods only classify manually segmented single chromosome, which is far from clinical practice. In this work, we propose a detection based method, DeepACC, to locate and fine classify chromosomes simultaneously based on the whole metaphase image. We firstly introduce the Additive Angular Margin Loss to enhance the discriminative power of model. To alleviate batch effects, we transform decision boundary of each class case-by-case through a siamese network which make full use of prior knowledges that chromosomes usually appear in pairs. Furthermore, we take the clinically seven group criterion as a prior knowledge and design an additional Group Inner-Adjacency Loss to further reduce inter-class similarities. 3390 metaphase images from clinical laboratory are collected and labelled to evaluate the performance. Results show that the new design brings encouraging performance gains comparing to the state-of-the-art baselines.

Li Xiao, Yufan Luo, Chunlong Luo et al.

Many recently developed object detectors focused on coarse-to-fine framework which contains several stages that classify and regress proposals from coarse-grain to fine-grain, and obtains more accurate detection gradually. Multi-resolution models such as Feature Pyramid Network(FPN) integrate information of different levels of resolution and effectively improve the performance. Previous researches also have revealed that localization can be further improved by: 1) using fine-grained information which is more translational variant; 2) refining local areas which is more focused on local boundary information. Based on these principles, we designed a novel boundary refinement architecture to improve localization accuracy by combining coarse-to-fine framework with feature pyramid structure, named as Pyramidal Bounding Box Refinement network(PBRnet), which parameterizes gradually focused boundary areas of objects and leverages lower-level feature maps to extract finer local information when refining the predicted bounding boxes. Extensive experiments are performed on the MS-COCO dataset. The PBRnet brings a significant performance gains by roughly 3 point of $mAP$ when added to FPN or Libra R-CNN. Moreover, by treating Cascade R-CNN as a coarse-to-fine detector and replacing its localization branch by the regressor of PBRnet, it leads an extra performance improvement by 1.5 $mAP$, yielding a total performance boosting by as high as 5 point of $mAP$.

Li Xiao, Chunlong Luo, Tianqi Yu et al.

Chromosome enumeration is an essential but tedious procedure in karyotyping analysis. To automate the enumeration process, we develop a chromosome enumeration framework, DeepACEv2, based on the region based object detection scheme. The framework is developed following three steps. Firstly, we take the classical ResNet-101 as the backbone and attach the Feature Pyramid Network (FPN) to the backbone. The FPN takes full advantage of the multiple level features, and we only output the level of feature map that most of the chromosomes are assigned to. Secondly, we enhance the region proposal network's ability by adding a newly proposed Hard Negative Anchors Sampling to extract unapparent but essential information about highly confusing partial chromosomes. Next, to alleviate serious occlusion problems, besides the traditional detection branch, we novelly introduce an isolated Template Module branch to extract unique embeddings of each proposal by utilizing the chromosome's geometric information. The embeddings are further incorporated into the No Maximum Suppression (NMS) procedure to improve the detection of overlapping chromosomes. Finally, we design a Truncated Normalized Repulsion Loss and add it to the loss function to avoid inaccurate localization caused by occlusion. In the newly collected 1375 metaphase images that came from a clinical laboratory, a series of ablation studies validate the effectiveness of each proposed module. Combining them, the proposed DeepACEv2 outperforms all the previous methods, yielding the Whole Correct Ratio(WCR)(%) with respect to images as 71.39, and the Average Error Ratio(AER)(%) with respect to chromosomes as about 1.17.