scholarly journals Robust Nucleus/Cell Detection and Segmentation in Digital Pathology and Microscopy Images: A Comprehensive Review

2016 ◽  
Vol 9 ◽  
pp. 234-263 ◽  
Author(s):  
Fuyong Xing ◽  
Lin Yang
2019 ◽  
Vol 20 (1) ◽  
Author(s):  
Fuyong Xing ◽  
Yuanpu Xie ◽  
Xiaoshuang Shi ◽  
Pingjun Chen ◽  
Zizhao Zhang ◽  
...  

Abstract Background Nucleus or cell detection is a fundamental task in microscopy image analysis and supports many other quantitative studies such as object counting, segmentation, tracking, etc. Deep neural networks are emerging as a powerful tool for biomedical image computing; in particular, convolutional neural networks have been widely applied to nucleus/cell detection in microscopy images. However, almost all models are tailored for specific datasets and their applicability to other microscopy image data remains unknown. Some existing studies casually learn and evaluate deep neural networks on multiple microscopy datasets, but there are still several critical, open questions to be addressed. Results We analyze the applicability of deep models specifically for nucleus detection across a wide variety of microscopy image data. More specifically, we present a fully convolutional network-based regression model and extensively evaluate it on large-scale digital pathology and microscopy image datasets, which consist of 23 organs (or cancer diseases) and come from multiple institutions. We demonstrate that for a specific target dataset, training with images from the same types of organs might be usually necessary for nucleus detection. Although the images can be visually similar due to the same staining technique and imaging protocol, deep models learned with images from different organs might not deliver desirable results and would require model fine-tuning to be on a par with those trained with target data. We also observe that training with a mixture of target and other/non-target data does not always mean a higher accuracy of nucleus detection, and it might require proper data manipulation during model training to achieve good performance. Conclusions We conduct a systematic case study on deep models for nucleus detection in a wide variety of microscopy images, aiming to address several important but previously understudied questions. We present and extensively evaluate an end-to-end, pixel-to-pixel fully convolutional regression network and report a few significant findings, some of which might have not been reported in previous studies. The model performance analysis and observations would be helpful to nucleus detection in microscopy images.


2018 ◽  
Vol 21 (6) ◽  
pp. 1721-1743 ◽  
Author(s):  
Xipeng Pan ◽  
Dengxian Yang ◽  
Lingqiao Li ◽  
Zhenbing Liu ◽  
Huihua Yang ◽  
...  

2017 ◽  
Vol 282 ◽  
pp. 20-33 ◽  
Author(s):  
Maryana Alegro ◽  
Panagiotis Theofilas ◽  
Austin Nguy ◽  
Patricia A. Castruita ◽  
William Seeley ◽  
...  

2021 ◽  
Author(s):  
Zhenbo Ren ◽  
Edmund Y. Lam ◽  
Jianlin Zhao

2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Lei Chen ◽  
Jianhua Zhang ◽  
Shengyong Chen ◽  
Yao Lin ◽  
Chunyan Yao ◽  
...  

Phase contrast microscope is one of the most universally used instruments to observe long-term cell movements in different solutions. Most of classic segmentation methods consider a homogeneous patch as an object, while the recorded cell images have rich details and a lot of small inhomogeneous patches, as well as some artifacts, which can impede the applications. To tackle these challenges, this paper presents a hierarchical mergence approach (HMA) to extract homogeneous patches out and heuristically add them up. Initially, the maximum region of interest (ROI), in which only cell events exist, is drawn by using gradient information as a mask. Then, different levels of blurring based on kernel or grayscale morphological operations are applied to the whole image to produce reference images. Next, each of unconnected regions in the mask is applied with Otsu method independently according to different reference images. Consequently, the segmentation result is generated by the combination of usable patches in all informative layers. The proposed approach is more than simply a fusion of the basic segmentation methods, but a well-organized strategy that integrates these basic methods. Experiments demonstrate that the proposed method outperforms previous methods within our datasets.


2020 ◽  
pp. 1-6
Author(s):  
Gray JC ◽  
Dalia Hammouche ◽  
Easton AS ◽  
Lopez MA ◽  
Taylor J ◽  
...  

This is a description of a novel combination of chromogenic multiplex immunohistochemistry, digital pathology, computer-aided cell detection and topographical analysis of tumor tissue to allow a detailed study of the immune infiltrate. This is applied to a rare clinical case, where a tumor sample is available from an infant with metastatic neuroblastoma at the point of spontaneous regression. This allowed detailed analysis of the immune infiltrate, including spatial distribution and phenotype of lymphoid and myeloid populations, with a distinction between heterogeneous areas within the intra- and extra- tumoral immune microenvironments. The mechanism of spontaneous regression in congenital neuroblastoma is poorly understood, but the data obtained suggested an immune-mediated phenomenon, characterised by an adaptive T cell driven response with a significant delayed-type hypersensitivity (granulomatous) component.


2020 ◽  
Vol 63 ◽  
pp. 101720 ◽  
Author(s):  
Can Fahrettin Koyuncu ◽  
Gozde Nur Gunesli ◽  
Rengul Cetin-Atalay ◽  
Cigdem Gunduz-Demir

2017 ◽  
Author(s):  
Ilida Suleymanova ◽  
Tamas Balassa ◽  
Sushil Tripathi ◽  
Csaba Molnar ◽  
Mart Saarma ◽  
...  

AbstractAstrocytes are involved in brain pathologies such as trauma or stroke, neurodegenerative disorders like Alzheimer’s and Parkinson’s disease, chronic pain, and many others. Determining cell density and timing of morphological and biochemical changes is important for a proper understanding of the role of astrocytes in physiological and pathological conditions. One of the most important of such analyses is astrocytes count within a complex tissue environment in microscopy images. The most widely used approaches for the quantification of microscopy images data are either manual stereological cell counting or semi-automatic segmentation techniques. Detecting astrocytes automatically is a highly challenging computational task, for which we currently lack efficient image analysis tools. In this study, we developed a fast and fully automated software that assesses the number of astrocytes using Deep Convolutional Neural Networks (DCNN). The method highly outperforms state-of-the-art image analysis and machine learning methods and provides detection accuracy and precision comparable to that of human experts. Additionally, the runtime of cell detection is significantly less than other three analyzed computational methods, and it is faster than human observers by orders of magnitude. We applied DCNN-based method to examine the number of astrocytes in different brain regions of rats with opioid-induced hyperalgesia/tolerance (OIH/OIT) as morphine tolerance is believed to activate glial cells in the brain. We observed strong positive correlation between manual cell detection and DCNN-based analysis method for counting astrocytes in the brains of experimental animals.


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