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Browsing by Author "Wu, Liming"
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Item 3D Centroidnet: Nuclei Centroid Detection with Vector Flow Voting(IEEE, 2022-10) Wu, Liming; Chen, Alain; Salama, Paul; Dunn, Kenneth W.; Delp, Edward J.; Electrical and Computer Engineering, School of Engineering and TechnologyAutomated microscope systems are increasingly used to collect large-scale 3D image volumes of biological tissues. Since cell boundaries are seldom delineated in these images, detection of nuclei is a critical step for identifying and analyzing individual cells. Due to the large intra-class variability in nuclei morphology and the difficulty of generating ground truth annotations, accurate nuclei detection remains a challenging task. We propose a 3D nuclei centroid detection method by estimating the "vector flow" volume where each voxel represents a 3D vector pointing to its nearest nuclei centroid in the corresponding microscopy volume. We then use a voting mechanism to estimate the 3D nuclei centroids from the "vector flow" volume. Our system is trained on synthetic microscopy volumes and tested on real microscopy volumes. The evaluation results indicate our method outperforms other methods both visually and quantitatively.Item An Ensemble Learning and Slice Fusion Strategy for Three-Dimensional Nuclei Instance Segmentation(IEEE, 2022-06) Wu, Liming; Chen, Alain; Salama, Paul; Dunn, Kenneth W.; Delp, Edward J.; Electrical and Computer Engineering, School of Engineering and TechnologyAutomated microscopy image analysis is a fundamental step for digital pathology and computer aided diagnosis. Most existing deep learning methods typically require post-processing to achieve instance segmentation and are computationally expensive when directly used with 3D microscopy volumes. Supervised learning methods generally need large amounts of ground truth annotations for training whereas manually annotating ground truth masks is laborious especially for a 3D volume. To address these issues, we propose an ensemble learning and slice fusion strategy for 3D nuclei instance segmentation that we call Ensemble Mask R-CNN (EMR-CNN) which uses different object detectors to generate nuclei segmentation masks for each 2D slice of a volume and propose a 2D ensemble fusion and a 2D to 3D slice fusion to merge these 2D segmentation masks into a 3D segmentation mask. Our method does not need any ground truth annotations for training and can inference on any large size volumes. Our proposed method was tested on a variety of microscopy volumes collected from multiple regions of organ tissues. The execution time and robustness analyses show that our method is practical and effective.Item DINAVID: A Distributed and Networked Image Analysis System for Volumetric Image Data(Cold Spring Harbor Laboratory, 2022-05-11) Han, Shuo; Chen , Alain; Lee, Soonam; Fu, Chichen; Yang, Changye; Wu, Liming; Winfree, Seth; El-Achkar, Tarek M.; Dunn, Kenneth W.; Salama, Paul; Delp, Edward J.; Electrical and Computer Engineering, School of Engineering and TechnologyBackground: The advancement of high content optical microscopy has enabled the acquisition of very large 3D image datasets. Image analysis tools and three dimensional visualization are critical for analyzing and interpreting 3D image volumes. The analysis of these volumes require more computational resources than a biologist may have access to in typical desktop or laptop computers. This is especially true if machine learning tools are being used for image analysis. With the increased amount of data analysis and computational complexity, there is a need for a more accessible, easy-to-use, and efficient network-based/cloud-based 3D image processing system. Results: The Distributed and Networked Analysis of Volumetric Image Data (DINAVID) system was developed to enable remote analysis of 3D microscopy images for biologists. DINAVID is a server/cloud-based system with a simple web interface that allows biologists to upload 3D volumes for analysis and visualization. DINAVID is designed using open source tools and has two main sub-systems, a computational system for 3D microscopy image processing and analysis as well as a 3D visualization system. Conclusions: In this paper, we will present an overview of the DINAVID system and compare it to other tools currently available for microscopy image analysis.Item NISNet3D: three-dimensional nuclear synthesis and instance segmentation for fluorescence microscopy images(Springer Nature, 2023-06-12) Wu, Liming; Chen, Alain; Salama, Paul; Winfree, Seth; Dunn, Kenneth W.; Delp, Edward J.; Electrical and Computer Engineering, School of Engineering and TechnologyThe primary step in tissue cytometry is the automated distinction of individual cells (segmentation). Since cell borders are seldom labeled, cells are generally segmented by their nuclei. While tools have been developed for segmenting nuclei in two dimensions, segmentation of nuclei in three-dimensional volumes remains a challenging task. The lack of effective methods for three-dimensional segmentation represents a bottleneck in the realization of the potential of tissue cytometry, particularly as methods of tissue clearing present the opportunity to characterize entire organs. Methods based on deep learning have shown enormous promise, but their implementation is hampered by the need for large amounts of manually annotated training data. In this paper, we describe 3D Nuclei Instance Segmentation Network (NISNet3D) that directly segments 3D volumes through the use of a modified 3D U-Net, 3D marker-controlled watershed transform, and a nuclei instance segmentation system for separating touching nuclei. NISNet3D is unique in that it provides accurate segmentation of even challenging image volumes using a network trained on large amounts of synthetic nuclei derived from relatively few annotated volumes, or on synthetic data obtained without annotated volumes. We present a quantitative comparison of results obtained from NISNet3D with results obtained from a variety of existing nuclei segmentation techniques. We also examine the performance of the methods when no ground truth is available and only synthetic volumes were used for training.Item RCNN-SliceNet: A Slice and Cluster Approach for Nuclei Centroid Detection in Three-Dimensional Fluorescence Microscopy Images(IEEE, 2021) Wu, Liming; Han, Shuo; Chen, Alain; Salama, Paul; Dunn, Kenneth W.; Delp, Edward J.; Electrical and Computer Engineering, School of Engineering and TechnologyRobust and accurate nuclei centroid detection is important for the understanding of biological structures in fluorescence microscopy images. Existing automated nuclei localization methods face three main challenges: (1) Most of object detection methods work only on 2D images and are difficult to extend to 3D volumes; (2) Segmentation-based models can be used on 3D volumes but it is computational expensive for large microscopy volumes and they have difficulty distinguishing different instances of objects; (3) Hand annotated ground truth is limited for 3D microscopy volumes. To address these issues, we present a scalable approach for nuclei centroid detection of 3D microscopy volumes. We describe the RCNN-SliceNet to detect 2D nuclei centroids for each slice of the volume from different directions and 3D agglomerative hierarchical clustering (AHC) is used to estimate the 3D centroids of nuclei in a volume. The model was trained with the synthetic microscopy data generated using Spatially Constrained Cycle-Consistent Adversarial Networks (SpCycle-GAN) and tested on different types of real 3D microscopy data. Extensive experimental results demonstrate that our proposed method can accurately count and detect the nuclei centroids in a 3D microscopy volume.