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In practice, digital pathology images are often affected by various factors, resulting in very large differences in color and brightness. Stain normalization can effectively reduce the differences in color and brightness of digital pathology images, thus improving the performance of computer-aided diagnostic systems. Conventional stain normalization methods rely on one or several reference images, but one or several images may not adequately represent the entire dataset. Although learning-based stain normalization methods are a general approach, they use complex deep networks, which not only greatly reduce computational efficiency, but also risk introducing artifacts. Some studies use specialized network structures to enhance computational efficiency and reliability, but these methods are difficult to apply to multi-to-one stain normalization due to insufficient network capacity. In this study, we introduced dynamic-parameter network and proposed a novel method for stain normalization, called ParamNet. ParamNet addresses the challenges of limited network capacity and computational efficiency by introducing dynamic parameters (weights and biases of convolutional layers) into the network design. By effectively leveraging these parameters, ParamNet achieves superior performance in stain normalization while maintaining computational efficiency. Results show ParamNet can normalize one whole slide image (WSI) of 100,000x100,000 within 25s. The code is available at: https://github.com/khtao/ParamNet.

Cervical glandular cell (GC) detection is a key step in computer-aided diagnosis for cervical adenocarcinomas screening. It is challenging to accurately recognize GCs in cervical smears in which squamous cells are the major. Widely existing Out-Of-Distribution (OOD) data in the entire smear leads decreasing reliability of machine learning system for GC detection. Although, the State-Of-The-Art (SOTA) deep learning model can outperform pathologists in preselected regions of interest, the mass False Positive (FP) prediction with high probability is still unsolved when facing such gigapixel whole slide image. This paper proposed a novel PolarNet based on the morphological prior knowledge of GC trying to solve the FP problem via a self-attention mechanism in eight-neighbor. It estimates the polar orientation of nucleus of GC. As a plugin module, PolarNet can guide the deep feature and predicted confidence of general object detection models. In experiments, we discovered that general models based on four different frameworks can reject FP in small image set and increase the mean of average precision (mAP) by $\text{0.007}\sim\text{0.015}$ in average, where the highest exceeds the recent cervical cell detection model 0.037. By plugging PolarNet, the deployed C++ program improved by 8.8\% on accuracy of top-20 GC detection from external WSIs, while sacrificing 14.4 s of computational time. Code is available in https://github.com/Chrisa142857/PolarNet-GCdet, Comment: 11 pages, 9 figures

Digital gigapixel whole slide image (WSI) is widely used in clinical diagnosis, and automated WSI analysis is key for computer-aided diagnosis. Currently, analyzing the integrated descriptor of probabilities or feature maps from massive local patches encoded by ResNet classifier is the main manner for WSI-level prediction. Feature representations of the sparse and tiny lesion cells in cervical slides, however, are still challenging, while the unused location representations are available to supply the semantics classification. This study designs a novel and efficient framework with a new module InCNet constructed lightweight model YOLCO (You Only Look Cytology Once). It directly extracts feature inside the single cell (cluster) instead of the traditional way that from image tile with a fixed size. The InCNet (Inline Connection Network) enriches the multi-scale connectivity without efficiency loss. The proposal allows the input size enlarged to megapixel that can stitch the WSI by the average repeats decreased from $10^3\sim10^4$ to $10^1\sim10^2$ for collecting features and predictions at two scales. Based on Transformer for classifying the integrated multi-scale multi-task WSI features, the experimental results appear $0.872$ AUC score better than the best conventional model on our dataset ($n$=2,019) from four scanners. The code is available at https://github.com/Chrisa142857/You-Only-Look-Cytopathology-Once , where the deployment version has the speed $\sim$70 s/WSI., Comment: 15 pages, 8 figures, under review to Medical Image Analysis (2nd round)

Stain normalization often refers to transferring the color distribution of the source image to that of the target image and has been widely used in biomedical image analysis. The conventional stain normalization is regarded as constructing a pixel-by-pixel color mapping model, which only depends on one reference image, and can not accurately achieve the style transformation between image datasets. In principle, this style transformation can be well solved by the deep learning-based methods due to its complicated network structure, whereas, its complicated structure results in the low computational efficiency and artifacts in the style transformation, which has restricted the practical application. Here, we use distillation learning to reduce the complexity of deep learning methods and a fast and robust network called StainNet to learn the color mapping between the source image and target image. StainNet can learn the color mapping relationship from a whole dataset and adjust the color value in a pixel-to-pixel manner. The pixel-to-pixel manner restricts the network size and avoids artifacts in the style transformation. The results on the cytopathology and histopathology datasets show that StainNet can achieve comparable performance to the deep learning-based methods. Computation results demonstrate StainNet is more than 40 times faster than StainGAN and can normalize a 100,000x100,000 whole slide image in 40 seconds., Comment: 14 pages, 8 figures

High-resolution 3D medical images are important for analysis and diagnosis, but axial scanning to acquire them is very time-consuming. In this paper, we propose a fast end-to-end multi-focal plane imaging network (MFPINet) to reconstruct high-resolution multi-focal plane images from a single 2D low-resolution wild filed image without relying on scanning. To acquire realistic MFP images fast, the proposed MFPINet adopts generative adversarial network framework and the strategies of post-sampling and refocusing all focal planes at one time. We conduct a series experiments on cytology microscopy images and demonstrate that MFPINet performs well on both axial refocusing and horizontal super resolution. Furthermore, MFPINet is approximately 24 times faster than current refocusing methods for reconstructing the same volume images. The proposed method has the potential to greatly increase the speed of high-resolution 3D imaging and expand the application of low-resolution wide-field images., Comment: 9 pages, 4 figures,3 Tables

Multi-focus image fusion technologies compress different focus depth images into an image in which most objects are in focus. However, although existing image fusion techniques, including traditional algorithms and deep learning-based algorithms, can generate high-quality fused images, they need multiple images with different focus depths in the same field of view. This criterion may not be met in some cases where time efficiency is required or the hardware is insufficient. The problem is especially prominent in large-size whole slide images. This paper focused on the multi-focus image fusion of cytopathological digital slide images, and proposed a novel method for generating fused images from single-focus or few-focus images based on conditional generative adversarial network (GAN). Through the adversarial learning of the generator and discriminator, the method is capable of generating fused images with clear textures and large depth of field. Combined with the characteristics of cytopathological images, this paper designs a new generator architecture combining U-Net and DenseBlock, which can effectively improve the network's receptive field and comprehensively encode image features. Meanwhile, this paper develops a semantic segmentation network that identifies the blurred regions in cytopathological images. By integrating the network into the generative model, the quality of the generated fused images is effectively improved. Our method can generate fused images from only single-focus or few-focus images, thereby avoiding the problem of collecting multiple images of different focus depths with increased time and hardware costs. Furthermore, our model is designed to learn the direct mapping of input source images to fused images without the need to manually design complex activity level measurements and fusion rules as in traditional methods.

The different stain styles of cytopathological images have a negative effect on the generalization ability of automated image analysis algorithms. This article proposes a new framework that normalizes the stain style for cytopathological images through a stain removal module and a multi-stage domain adversarial style reconstruction module. We convert colorful images into grayscale images with a color-encoding mask. Using the mask, reconstructed images retain their basic color without red and blue mixing, which is important for cytopathological image interpretation. The style reconstruction module consists of per-pixel regression with intradomain adversarial learning, inter-domain adversarial learning, and optional task-based refining. Per-pixel regression with intradomain adversarial learning establishes the generative network from the decolorized input to the reconstructed output. The interdomain adversarial learning further reduces the difference in stain style. The generation network can be optimized by combining it with the task network. Experimental results show that the proposed techniques help to optimize the generation network. The average accuracy increases from 75.41% to 84.79% after the intra-domain adversarial learning, and to 87.00% after interdomain adversarial learning. Under the guidance of the task network, the average accuracy rate reaches 89.58%. The proposed method achieves unsupervised stain normalization of cytopathological images, while preserving the cell structure, texture structure, and cell color properties of the image. This method overcomes the problem of generalizing the task models between different stain styles of cytopathological images.