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Effective automated pipeline for 3D reconstruction of synapses based on deep learning
BACKGROUND: The locations and shapes of synapses are important in reconstructing connectomes and analyzing synaptic plasticity. However, current synapse detection and segmentation methods are still not adequate for accurately acquiring the synaptic connectivity, and they cannot effectively alleviate...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044049/ https://www.ncbi.nlm.nih.gov/pubmed/30005590 http://dx.doi.org/10.1186/s12859-018-2232-0 |
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author | Xiao, Chi Li, Weifu Deng, Hao Chen, Xi Yang, Yang Xie, Qiwei Han, Hua |
author_facet | Xiao, Chi Li, Weifu Deng, Hao Chen, Xi Yang, Yang Xie, Qiwei Han, Hua |
author_sort | Xiao, Chi |
collection | PubMed |
description | BACKGROUND: The locations and shapes of synapses are important in reconstructing connectomes and analyzing synaptic plasticity. However, current synapse detection and segmentation methods are still not adequate for accurately acquiring the synaptic connectivity, and they cannot effectively alleviate the burden of synapse validation. RESULTS: We propose a fully automated method that relies on deep learning to realize the 3D reconstruction of synapses in electron microscopy (EM) images. The proposed method consists of three main parts: (1) training and employing the faster region convolutional neural networks (R-CNN) algorithm to detect synapses, (2) using the z-continuity of synapses to reduce false positives, and (3) combining the Dijkstra algorithm with the GrabCut algorithm to obtain the segmentation of synaptic clefts. Experimental results were validated by manual tracking, and the effectiveness of our proposed method was demonstrated. The experimental results in anisotropic and isotropic EM volumes demonstrate the effectiveness of our algorithm, and the average precision of our detection (92.8% in anisotropy, 93.5% in isotropy) and segmentation (88.6% in anisotropy, 93.0% in isotropy) suggests that our method achieves state-of-the-art results. CONCLUSIONS: Our fully automated approach contributes to the development of neuroscience, providing neurologists with a rapid approach for obtaining rich synaptic statistics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2232-0) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6044049 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-60440492018-07-13 Effective automated pipeline for 3D reconstruction of synapses based on deep learning Xiao, Chi Li, Weifu Deng, Hao Chen, Xi Yang, Yang Xie, Qiwei Han, Hua BMC Bioinformatics Methodology Article BACKGROUND: The locations and shapes of synapses are important in reconstructing connectomes and analyzing synaptic plasticity. However, current synapse detection and segmentation methods are still not adequate for accurately acquiring the synaptic connectivity, and they cannot effectively alleviate the burden of synapse validation. RESULTS: We propose a fully automated method that relies on deep learning to realize the 3D reconstruction of synapses in electron microscopy (EM) images. The proposed method consists of three main parts: (1) training and employing the faster region convolutional neural networks (R-CNN) algorithm to detect synapses, (2) using the z-continuity of synapses to reduce false positives, and (3) combining the Dijkstra algorithm with the GrabCut algorithm to obtain the segmentation of synaptic clefts. Experimental results were validated by manual tracking, and the effectiveness of our proposed method was demonstrated. The experimental results in anisotropic and isotropic EM volumes demonstrate the effectiveness of our algorithm, and the average precision of our detection (92.8% in anisotropy, 93.5% in isotropy) and segmentation (88.6% in anisotropy, 93.0% in isotropy) suggests that our method achieves state-of-the-art results. CONCLUSIONS: Our fully automated approach contributes to the development of neuroscience, providing neurologists with a rapid approach for obtaining rich synaptic statistics. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12859-018-2232-0) contains supplementary material, which is available to authorized users. BioMed Central 2018-07-13 /pmc/articles/PMC6044049/ /pubmed/30005590 http://dx.doi.org/10.1186/s12859-018-2232-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Methodology Article Xiao, Chi Li, Weifu Deng, Hao Chen, Xi Yang, Yang Xie, Qiwei Han, Hua Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title | Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title_full | Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title_fullStr | Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title_full_unstemmed | Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title_short | Effective automated pipeline for 3D reconstruction of synapses based on deep learning |
title_sort | effective automated pipeline for 3d reconstruction of synapses based on deep learning |
topic | Methodology Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6044049/ https://www.ncbi.nlm.nih.gov/pubmed/30005590 http://dx.doi.org/10.1186/s12859-018-2232-0 |
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