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BSCN: bidirectional symmetric cascade network for retinal vessel segmentation

BACKGROUND: Retinal blood vessel segmentation has an important guiding significance for the analysis and diagnosis of cardiovascular diseases such as hypertension and diabetes. But the traditional manual method of retinal blood vessel segmentation is not only time-consuming and laborious but also ca...

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Autores principales: Guo, Yanfei, Peng, Yanjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029442/
https://www.ncbi.nlm.nih.gov/pubmed/32070306
http://dx.doi.org/10.1186/s12880-020-0412-7
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author Guo, Yanfei
Peng, Yanjun
author_facet Guo, Yanfei
Peng, Yanjun
author_sort Guo, Yanfei
collection PubMed
description BACKGROUND: Retinal blood vessel segmentation has an important guiding significance for the analysis and diagnosis of cardiovascular diseases such as hypertension and diabetes. But the traditional manual method of retinal blood vessel segmentation is not only time-consuming and laborious but also cannot guarantee the accuracy and efficiency of diagnosis. Therefore, it is especially significant to create a computer-aided method of automatic and accurate retinal vessel segmentation. METHODS: In order to extract the blood vessels’ contours of different diameters to realize fine segmentation of retinal vessels, we propose a Bidirectional Symmetric Cascade Network (BSCN) where each layer is supervised by vessel contour labels of specific diameter scale instead of using one general ground truth to train different network layers. In addition, to increase the multi-scale feature representation of retinal blood vessels, we propose the Dense Dilated Convolution Module (DDCM), which extracts retinal vessel features of different diameters by adjusting the dilation rate in the dilated convolution branches and generates two blood vessel contour prediction results by two directions respectively. All dense dilated convolution module outputs are fused to obtain the final vessel segmentation results. RESULTS: We experimented the three datasets of DRIVE, STARE, HRF and CHASE_DB1, and the proposed method reaches accuracy of 0.9846/0.9872/0.9856/0.9889 and AUC of 0.9874/0.9941/0.9882/0.9874 on DRIVE, STARE, HRF and CHASE_DB1. CONCLUSIONS: The experimental results show that compared with the state-of-art methods, the proposed method has strong robustness, it not only avoids the adverse interference of the lesion background but also detects the tiny blood vessels at the intersection accurately.
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spelling pubmed-70294422020-02-25 BSCN: bidirectional symmetric cascade network for retinal vessel segmentation Guo, Yanfei Peng, Yanjun BMC Med Imaging Research Article BACKGROUND: Retinal blood vessel segmentation has an important guiding significance for the analysis and diagnosis of cardiovascular diseases such as hypertension and diabetes. But the traditional manual method of retinal blood vessel segmentation is not only time-consuming and laborious but also cannot guarantee the accuracy and efficiency of diagnosis. Therefore, it is especially significant to create a computer-aided method of automatic and accurate retinal vessel segmentation. METHODS: In order to extract the blood vessels’ contours of different diameters to realize fine segmentation of retinal vessels, we propose a Bidirectional Symmetric Cascade Network (BSCN) where each layer is supervised by vessel contour labels of specific diameter scale instead of using one general ground truth to train different network layers. In addition, to increase the multi-scale feature representation of retinal blood vessels, we propose the Dense Dilated Convolution Module (DDCM), which extracts retinal vessel features of different diameters by adjusting the dilation rate in the dilated convolution branches and generates two blood vessel contour prediction results by two directions respectively. All dense dilated convolution module outputs are fused to obtain the final vessel segmentation results. RESULTS: We experimented the three datasets of DRIVE, STARE, HRF and CHASE_DB1, and the proposed method reaches accuracy of 0.9846/0.9872/0.9856/0.9889 and AUC of 0.9874/0.9941/0.9882/0.9874 on DRIVE, STARE, HRF and CHASE_DB1. CONCLUSIONS: The experimental results show that compared with the state-of-art methods, the proposed method has strong robustness, it not only avoids the adverse interference of the lesion background but also detects the tiny blood vessels at the intersection accurately. BioMed Central 2020-02-18 /pmc/articles/PMC7029442/ /pubmed/32070306 http://dx.doi.org/10.1186/s12880-020-0412-7 Text en © The Author(s) 2020 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 Research Article
Guo, Yanfei
Peng, Yanjun
BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title_full BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title_fullStr BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title_full_unstemmed BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title_short BSCN: bidirectional symmetric cascade network for retinal vessel segmentation
title_sort bscn: bidirectional symmetric cascade network for retinal vessel segmentation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7029442/
https://www.ncbi.nlm.nih.gov/pubmed/32070306
http://dx.doi.org/10.1186/s12880-020-0412-7
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