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FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation
Colorectal cancer, also known as rectal cancer, is one of the most common forms of cancer, and it can be completely cured with early diagnosis. The most effective and objective method of screening and diagnosis is colonoscopy. Polyp segmentation plays a crucial role in the diagnosis and treatment of...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277544/ https://www.ncbi.nlm.nih.gov/pubmed/35845422 http://dx.doi.org/10.3389/fbioe.2022.799541 |
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author | Shi, Liantao Wang, Yufeng Li, Zhengguo Qiumiao, Wen |
author_facet | Shi, Liantao Wang, Yufeng Li, Zhengguo Qiumiao, Wen |
author_sort | Shi, Liantao |
collection | PubMed |
description | Colorectal cancer, also known as rectal cancer, is one of the most common forms of cancer, and it can be completely cured with early diagnosis. The most effective and objective method of screening and diagnosis is colonoscopy. Polyp segmentation plays a crucial role in the diagnosis and treatment of diseases related to the digestive system, providing doctors with detailed auxiliary boundary information during clinical analysis. To this end, we propose a novel light-weight feature refining and context-guided network (FRCNet) for real-time polyp segmentation. In this method, we first employed the enhanced context-calibrated module to extract the most discriminative features by developing long-range spatial dependence through a context-calibrated operation. This operation is helpful to alleviate the interference of background noise and effectively distinguish the target polyps from the background. Furthermore, we designed the progressive context-aware fusion module to dynamically capture multi-scale polyps by collecting multi-range context information. Finally, the multi-scale pyramid aggregation module was used to learn more representative features, and these features were fused to refine the segmented results. Extensive experiments on the Kvasir, ClinicDB, ColonDB, ETIS, and Endoscene datasets demonstrated the effectiveness of the proposed model. Specifically, FRCNet achieves an mIoU of 84.9% and mDice score of 91.5% on the Kvasir dataset with a model size of only 0.78 M parameters, outperforming state-of-the-art methods. Models and codes are available at the footnote. |
format | Online Article Text |
id | pubmed-9277544 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92775442022-07-14 FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation Shi, Liantao Wang, Yufeng Li, Zhengguo Qiumiao, Wen Front Bioeng Biotechnol Bioengineering and Biotechnology Colorectal cancer, also known as rectal cancer, is one of the most common forms of cancer, and it can be completely cured with early diagnosis. The most effective and objective method of screening and diagnosis is colonoscopy. Polyp segmentation plays a crucial role in the diagnosis and treatment of diseases related to the digestive system, providing doctors with detailed auxiliary boundary information during clinical analysis. To this end, we propose a novel light-weight feature refining and context-guided network (FRCNet) for real-time polyp segmentation. In this method, we first employed the enhanced context-calibrated module to extract the most discriminative features by developing long-range spatial dependence through a context-calibrated operation. This operation is helpful to alleviate the interference of background noise and effectively distinguish the target polyps from the background. Furthermore, we designed the progressive context-aware fusion module to dynamically capture multi-scale polyps by collecting multi-range context information. Finally, the multi-scale pyramid aggregation module was used to learn more representative features, and these features were fused to refine the segmented results. Extensive experiments on the Kvasir, ClinicDB, ColonDB, ETIS, and Endoscene datasets demonstrated the effectiveness of the proposed model. Specifically, FRCNet achieves an mIoU of 84.9% and mDice score of 91.5% on the Kvasir dataset with a model size of only 0.78 M parameters, outperforming state-of-the-art methods. Models and codes are available at the footnote. Frontiers Media S.A. 2022-06-29 /pmc/articles/PMC9277544/ /pubmed/35845422 http://dx.doi.org/10.3389/fbioe.2022.799541 Text en Copyright © 2022 Shi, Wang, Li and Qiumiao. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Bioengineering and Biotechnology Shi, Liantao Wang, Yufeng Li, Zhengguo Qiumiao, Wen FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title | FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title_full | FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title_fullStr | FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title_full_unstemmed | FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title_short | FRCNet: Feature Refining and Context-Guided Network for Efficient Polyp Segmentation |
title_sort | frcnet: feature refining and context-guided network for efficient polyp segmentation |
topic | Bioengineering and Biotechnology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9277544/ https://www.ncbi.nlm.nih.gov/pubmed/35845422 http://dx.doi.org/10.3389/fbioe.2022.799541 |
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