scholarly journals A Pipeline for Neuron Reconstruction Based on Spatial Sliding Volume Filter Seeding

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Dong Sui ◽  
Kuanquan Wang ◽  
Jinseok Chae ◽  
Yue Zhang ◽  
Henggui Zhang

Neuron’s shape and dendritic architecture are important for biosignal transduction in neuron networks. And the anatomy architecture reconstruction of neuron cell is one of the foremost challenges and important issues in neuroscience. Accurate reconstruction results can facilitate the subsequent neuron system simulation. With the development of confocal microscopy technology, researchers can scan neurons at submicron resolution for experiments. These make the reconstruction of complex dendritic trees become more feasible; however, it is still a tedious, time consuming, and labor intensity task. For decades, computer aided methods have been playing an important role in this task, but none of the prevalent algorithms can reconstruct full anatomy structure automatically. All of these make it essential for developing new method for reconstruction. This paper proposes a pipeline with a novel seeding method for reconstructing neuron structures from 3D microscopy images stacks. The pipeline is initialized with a set of seeds detected by sliding volume filter (SVF), and then the open curve snake is applied to the detected seeds for reconstructing the full structure of neuron cells. The experimental results demonstrate that the proposed pipeline exhibits excellent performance in terms of accuracy compared with traditional method, which is clearly a benefit for 3D neuron detection and reconstruction.

Author(s):  
Yue Guo ◽  
Oleh Krupa ◽  
Jason Stein ◽  
Guorong Wu ◽  
Ashok Krishnamurthy

2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Grzegorz Bokota ◽  
Jacek Sroka ◽  
Subhadip Basu ◽  
Nirmal Das ◽  
Pawel Trzaskoma ◽  
...  

Abstract Background Bioimaging techniques offer a robust tool for studying molecular pathways and morphological phenotypes of cell populations subjected to various conditions. As modern high-resolution 3D microscopy provides access to an ever-increasing amount of high-quality images, there arises a need for their analysis in an automated, unbiased, and simple way. Segmentation of structures within the cell nucleus, which is the focus of this paper, presents a new layer of complexity in the form of dense packing and significant signal overlap. At the same time, the available segmentation tools provide a steep learning curve for new users with a limited technical background. This is especially apparent in the bulk processing of image sets, which requires the use of some form of programming notation. Results In this paper, we present PartSeg, a tool for segmentation and reconstruction of 3D microscopy images, optimised for the study of the cell nucleus. PartSeg integrates refined versions of several state-of-the-art algorithms, including a new multi-scale approach for segmentation and quantitative analysis of 3D microscopy images. The features and user-friendly interface of PartSeg were carefully planned with biologists in mind, based on analysis of multiple use cases and difficulties encountered with other tools, to offer an ergonomic interface with a minimal entry barrier. Bulk processing in an ad-hoc manner is possible without the need for programmer support. As the size of datasets of interest grows, such bulk processing solutions become essential for proper statistical analysis of results. Advanced users can use PartSeg components as a library within Python data processing and visualisation pipelines, for example within Jupyter notebooks. The tool is extensible so that new functionality and algorithms can be added by the use of plugins. For biologists, the utility of PartSeg is presented in several scenarios, showing the quantitative analysis of nuclear structures. Conclusions In this paper, we have presented PartSeg which is a tool for precise and verifiable segmentation and reconstruction of 3D microscopy images. PartSeg is optimised for cell nucleus analysis and offers multi-scale segmentation algorithms best-suited for this task. PartSeg can also be used for the bulk processing of multiple images and its components can be reused in other systems or computational experiments.


2021 ◽  
Author(s):  
Hemaxi Narotamo ◽  
Marie Ouarne ◽  
Claudio Areias Franco ◽  
Margarida Silveira

SPIE Newsroom ◽  
2015 ◽  
Author(s):  
Manuel Martínez-Corral ◽  
Ana Doblas ◽  
Emilio Sánchez-Ortiga ◽  
Jorge Sola-Pikabea ◽  
Genaro Saavedra

2010 ◽  
Author(s):  
Stefan Wörz ◽  
Petra Sander ◽  
Martin Pfannmöller ◽  
Ralf J. Rieker ◽  
Stefan Joos ◽  
...  

2017 ◽  
Author(s):  
Gregory R. Johnson ◽  
Rory M. Donovan-Maiye ◽  
Mary M. Maleckar

AbstractWe present a conditional generative model for learning variation in cell and nuclear morphology and predicting the location of subcellular structures from 3D microscopy images. The model generalizes well to a wide array of structures and allows for a probabilistic interpretation of cell and nuclear morphology and structure localization from fluorescence images. We demonstrate the effectiveness of the approach by producing and evaluating photo-realistic 3D cell images using the generative model, and show that the conditional nature of the model provides the ability to predict the localization of unobserved structures, given cell and nuclear morphology. We additionally explore the model’s utility in a number of applications, including cellular integration from multiple experiments and exploration of variation in structure localization. Finally, we discuss the model in the context of foundational and contemporary work and suggest forthcoming extensions.


2015 ◽  
Author(s):  
Jian Mu ◽  
Lin Yang ◽  
Malgorzata M. Kamocka ◽  
Amy L. Zollman ◽  
Nadia Carlesso ◽  
...  

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