MRANet:用于息肉精确分割的多维残差注意网络

IF 1.9 4区 生物学 Q4 CELL BIOLOGY
Li Zhang, Yu Zeng, Yange Sun, Chengyi Zheng, Yan Feng, Huaping Guo
{"title":"MRANet:用于息肉精确分割的多维残差注意网络","authors":"Li Zhang,&nbsp;Yu Zeng,&nbsp;Yange Sun,&nbsp;Chengyi Zheng,&nbsp;Yan Feng,&nbsp;Huaping Guo","doi":"10.1049/syb2.70031","DOIUrl":null,"url":null,"abstract":"<p>Automated polyp detection plays a critical role in the early diagnosis of colorectal cancer, ranking as the second leading cause of cancer-related mortality worldwide. However, existing segmentation methods face difficulties in handling complex polyp shapes, size variations, and generalising across diverse datasets. We propose a Multi-dimensional Residual Attention Network (MRANet) for the polyp segmentation task, focusing on enhancing feature representation and ensuring robust performance across diverse clinical scenarios. During encoding, MRANet employs residual self-attention to capture semantic information of high-level features, guiding the refinement of low-level information. In addition, convolutions with Multiple Kernel and Dilation rates (CMKD) are integrated with residual channel and spatial attentions to expand the model's receptive field, enhance encoder features, and accelerate convergence. In the decoding stage, MRANet uses the proposed Attention-based Scale Interaction Module (ASIM) to merge upsampled high-level features with low-level pixel information, enriching low-level layers using semantic knowledge. A Residual-based Scale Fusion Module (RSFM) is further designed to merge low-level features, which preserves high-frequency details including edges and textures. Experiments demonstrate that MRANet effectively segments polyps with varying sizes, indistinct boundaries, and scattered distributions, achieving the best overall performance. Our code is available at https://github.com/hpguo1982/MRANet.</p>","PeriodicalId":50379,"journal":{"name":"IET Systems Biology","volume":"19 1","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-08-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ietresearch.onlinelibrary.wiley.com/doi/epdf/10.1049/syb2.70031","citationCount":"0","resultStr":"{\"title\":\"MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation\",\"authors\":\"Li Zhang,&nbsp;Yu Zeng,&nbsp;Yange Sun,&nbsp;Chengyi Zheng,&nbsp;Yan Feng,&nbsp;Huaping Guo\",\"doi\":\"10.1049/syb2.70031\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>Automated polyp detection plays a critical role in the early diagnosis of colorectal cancer, ranking as the second leading cause of cancer-related mortality worldwide. However, existing segmentation methods face difficulties in handling complex polyp shapes, size variations, and generalising across diverse datasets. We propose a Multi-dimensional Residual Attention Network (MRANet) for the polyp segmentation task, focusing on enhancing feature representation and ensuring robust performance across diverse clinical scenarios. During encoding, MRANet employs residual self-attention to capture semantic information of high-level features, guiding the refinement of low-level information. In addition, convolutions with Multiple Kernel and Dilation rates (CMKD) are integrated with residual channel and spatial attentions to expand the model's receptive field, enhance encoder features, and accelerate convergence. In the decoding stage, MRANet uses the proposed Attention-based Scale Interaction Module (ASIM) to merge upsampled high-level features with low-level pixel information, enriching low-level layers using semantic knowledge. A Residual-based Scale Fusion Module (RSFM) is further designed to merge low-level features, which preserves high-frequency details including edges and textures. Experiments demonstrate that MRANet effectively segments polyps with varying sizes, indistinct boundaries, and scattered distributions, achieving the best overall performance. Our code is available at https://github.com/hpguo1982/MRANet.</p>\",\"PeriodicalId\":50379,\"journal\":{\"name\":\"IET Systems Biology\",\"volume\":\"19 1\",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-08-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://ietresearch.onlinelibrary.wiley.com/doi/epdf/10.1049/syb2.70031\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IET Systems Biology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://ietresearch.onlinelibrary.wiley.com/doi/10.1049/syb2.70031\",\"RegionNum\":4,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IET Systems Biology","FirstCategoryId":"99","ListUrlMain":"https://ietresearch.onlinelibrary.wiley.com/doi/10.1049/syb2.70031","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

自动息肉检测在结直肠癌的早期诊断中起着至关重要的作用,结直肠癌是全球癌症相关死亡的第二大原因。然而,现有的分割方法在处理复杂的息肉形状、大小变化和跨不同数据集的泛化方面面临困难。我们提出了一个用于息肉分割任务的多维剩余注意网络(MRANet),重点是增强特征表示并确保在不同临床场景下的稳健性能。在编码过程中,MRANet利用残差自注意捕获高级特征的语义信息,指导低级信息的细化。此外,将多核膨胀率卷积(Multiple Kernel and Dilation rates, cmcd)与残差通道和空间关注相结合,扩展模型的接受域,增强编码器特征,加快收敛速度。在解码阶段,MRANet使用提出的基于注意力的尺度交互模块(ASIM)将上采样的高级特征与低级像素信息合并,使用语义知识丰富低级层。进一步设计了基于残差的尺度融合模块(RSFM)来融合低阶特征,保留了包括边缘和纹理在内的高频细节。实验表明,MRANet能有效分割大小不一、边界模糊、分布分散的息肉,达到最佳的综合性能。我们的代码可在https://github.com/hpguo1982/MRANet上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation

MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation

MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation

MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation

MRANet: Multi-Dimensional Residual Attentional Network for Precise Polyp Segmentation

Automated polyp detection plays a critical role in the early diagnosis of colorectal cancer, ranking as the second leading cause of cancer-related mortality worldwide. However, existing segmentation methods face difficulties in handling complex polyp shapes, size variations, and generalising across diverse datasets. We propose a Multi-dimensional Residual Attention Network (MRANet) for the polyp segmentation task, focusing on enhancing feature representation and ensuring robust performance across diverse clinical scenarios. During encoding, MRANet employs residual self-attention to capture semantic information of high-level features, guiding the refinement of low-level information. In addition, convolutions with Multiple Kernel and Dilation rates (CMKD) are integrated with residual channel and spatial attentions to expand the model's receptive field, enhance encoder features, and accelerate convergence. In the decoding stage, MRANet uses the proposed Attention-based Scale Interaction Module (ASIM) to merge upsampled high-level features with low-level pixel information, enriching low-level layers using semantic knowledge. A Residual-based Scale Fusion Module (RSFM) is further designed to merge low-level features, which preserves high-frequency details including edges and textures. Experiments demonstrate that MRANet effectively segments polyps with varying sizes, indistinct boundaries, and scattered distributions, achieving the best overall performance. Our code is available at https://github.com/hpguo1982/MRANet.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
IET Systems Biology
IET Systems Biology 生物-数学与计算生物学
CiteScore
4.20
自引率
4.30%
发文量
17
审稿时长
>12 weeks
期刊介绍: IET Systems Biology covers intra- and inter-cellular dynamics, using systems- and signal-oriented approaches. Papers that analyse genomic data in order to identify variables and basic relationships between them are considered if the results provide a basis for mathematical modelling and simulation of cellular dynamics. Manuscripts on molecular and cell biological studies are encouraged if the aim is a systems approach to dynamic interactions within and between cells. The scope includes the following topics: Genomics, transcriptomics, proteomics, metabolomics, cells, tissue and the physiome; molecular and cellular interaction, gene, cell and protein function; networks and pathways; metabolism and cell signalling; dynamics, regulation and control; systems, signals, and information; experimental data analysis; mathematical modelling, simulation and theoretical analysis; biological modelling, simulation, prediction and control; methodologies, databases, tools and algorithms for modelling and simulation; modelling, analysis and control of biological networks; synthetic biology and bioengineering based on systems biology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信