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Cell segmentation is essential in biomedical research for analyzing cellular morphology and behavior. Deep learning methods, particularly convolutional neural networks (CNNs), have revolutionized cell segmentation by extracting intricate features from images. However, the robustness of these methods under microscope optical aberrations remains a critical challenge. This study evaluates cell image segmentation models under optical aberrations from fluorescence and bright field microscopy. By simulating different types of aberrations, including astigmatism, coma, spherical aberration, trefoil, and mixed aberrations, we conduct a thorough evaluation of various cell instance segmentation models using the DynamicNuclearNet (DNN) and LIVECell datasets, representing fluorescence and bright field microscopy cell datasets, respectively. We train and test several segmentation models, including the Otsu threshold method and Mask R-CNN with different network heads (FPN, C3) and backbones (ResNet, VGG, Swin Transformer), under aberrated conditions. Additionally, we provide usage recommendations for the Cellpose 2.0 Toolbox on complex cell degradation images. The results indicate that the combination of FPN and SwinS demonstrates superior robustness in handling simple cell images affected by minor aberrations. In contrast, Cellpose 2.0 proves effective for complex cell images under similar conditions. Furthermore, we innovatively propose the Point Spread Function Image Label Classification Model (PLCM). This model can quickly and accurately identify aberration types and amplitudes from PSF images, assisting researchers without optical training. Through PLCM, researchers can better apply our proposed cell segmentation guidelines.

The precise spatial and quantitative delineation of indistinct-boundary medical objects is paramount for the accuracy of diagnostic protocols, efficacy of surgical interventions, and reliability of postoperative assessments. Despite their significance, the effective segmentation and instantaneous three-dimensional reconstruction are significantly impeded by the paucity of representative samples in available datasets and noise artifacts. To surmount these challenges, we introduced Stochastic Defect Injection (SDi) to augment the representational diversity of challenging indistinct-boundary objects within training corpora. Consequently, we propose the Dual-Encoder Fourier Group Harmonics Network (DEFN) to tailor noise filtration, amplify detailed feature recognition, and bolster representation across diverse medical imaging scenarios. By incorporating Dynamic Weight Composing (DWC) loss dynamically adjusts model's focus based on training progression, DEFN achieves SOTA performance on the OIMHS public dataset, showcasing effectiveness in indistinct boundary contexts. Source code for DEFN is available at: https://github.com/IMOP-lab/DEFN-pytorch., Comment: 36pages,16figures,7tables

Cancer segmentation in whole-slide images is a fundamental step for viable tumour burden estimation, which is of great value for cancer assessment. However, factors like vague boundaries or small regions dissociated from viable tumour areas make it a challenging task. Considering the usefulness of multi-scale features in various vision-related tasks, we present a structure-aware scale-adaptive feature selection method for efficient and accurate cancer segmentation. Based on a segmentation network with a popular encoder-decoder architecture, a scale-adaptive module is proposed for selecting more robust features to represent the vague, non-rigid boundaries. Furthermore, a structural similarity metric is proposed for better tissue structure awareness to deal with small region segmentation. In addition, advanced designs including several attention mechanisms and the selective-kernel convolutions are applied to the baseline network for comparative study purposes. Extensive experimental results show that the proposed structure-aware scale-adaptive networks achieve outstanding performance on liver cancer segmentation when compared to top ten submitted results in the challenge of PAIP 2019. Further evaluation on colorectal cancer segmentation shows that the scale-adaptive module improves the baseline network or outperforms the other excellent designs of attention mechanisms when considering the tradeoff between efficiency and accuracy.

The classification of histopathological images is of great value in both cancer diagnosis and pathological studies. However, multiple reasons, such as variations caused by magnification factors and class imbalance, make it a challenging task where conventional methods that learn from image-label datasets perform unsatisfactorily in many cases. We observe that tumours of the same class often share common morphological patterns. To exploit this fact, we propose an approach that learns similarity-based multi-scale embeddings (SMSE) for magnification-independent histopathological image classification. In particular, a pair loss and a triplet loss are leveraged to learn similarity-based embeddings from image pairs or image triplets. The learned embeddings provide accurate measurements of similarities between images, which are regarded as a more effective form of representation for histopathological morphology than normal image features. Furthermore, in order to ensure the generated models are magnification-independent, images acquired at different magnification factors are simultaneously fed to networks during training for learning multi-scale embeddings. In addition to the SMSE, to eliminate the impact of class imbalance, instead of using the hard sample mining strategy that intuitively discards some easy samples, we introduce a new reinforced focal loss to simultaneously punish hard misclassified samples while suppressing easy well-classified samples. Experimental results show that the SMSE improves the performance for histopathological image classification tasks for both breast and liver cancers by a large margin compared to previous methods. In particular, the SMSE achieves the best performance on the BreakHis benchmark with an improvement ranging from 5% to 18% compared to previous methods using traditional features., Comment: more experiments and author list updated

The detection of nuclei and cells in histology images is of great value in both clinical practice and pathological studies. However, multiple reasons such as morphological variations of nuclei or cells make it a challenging task where conventional object detection methods cannot obtain satisfactory performance in many cases. A detection task consists of two sub-tasks, classification and localization. Under the condition of dense object detection, classification is a key to boost the detection performance. Considering this, we propose similarity based region proposal networks (SRPN) for nuclei and cells detection in histology images. In particular, a customized convolution layer termed as embedding layer is designed for network building. The embedding layer is added into the region proposal networks, enabling the networks to learn discriminative features based on similarity learning. Features obtained by similarity learning can significantly boost the classification performance compared to conventional methods. SRPN can be easily integrated into standard convolutional neural networks architectures such as the Faster R-CNN and RetinaNet. We test the proposed approach on tasks of multi-organ nuclei detection and signet ring cells detection in histological images. Experimental results show that networks applying similarity learning achieved superior performance on both tasks when compared to their counterparts. In particular, the proposed SRPN achieve state-of-the-art performance on the MoNuSeg benchmark for nuclei segmentation and detection while compared to previous methods, and on the signet ring cell detection benchmark when compared with baselines. The sourcecode is publicly available at: https://github.com/sigma10010/nuclei_cells_det., Comment: Accepted by Medical Image Analysis for publication

Histopathological cancer diagnosis is based on visual examination of stained tissue slides. Hematoxylin and eosin (H\&E) is a standard stain routinely employed worldwide. It is easy to acquire and cost effective, but cells and tissue components show low-contrast with varying tones of dark blue and pink, which makes difficult visual assessments, digital image analysis, and quantifications. These limitations can be overcome by IHC staining of target proteins of the tissue slide. IHC provides a selective, high-contrast imaging of cells and tissue components, but their use is largely limited by a significantly more complex laboratory processing and high cost. We proposed a conditional CycleGAN (cCGAN) network to transform the H\&E stained images into IHC stained images, facilitating virtual IHC staining on the same slide. This data-driven method requires only a limited amount of labelled data but will generate pixel level segmentation results. The proposed cCGAN model improves the original network \cite{zhu_unpaired_2017} by adding category conditions and introducing two structural loss functions, which realize a multi-subdomain translation and improve the translation accuracy as well. % need to give reasons here. Experiments demonstrate that the proposed model outperforms the original method in unpaired image translation with multi-subdomains. We also explore the potential of unpaired images to image translation method applied on other histology images related tasks with different staining techniques.