Dopcc:通过多指标和共核附着法检测重叠蛋白质复合物。

IF 3.6 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Wenkang Wang, Xiangmao Meng, Ju Xiang, Hayat Dino Bedru, Min Li
{"title":"Dopcc:通过多指标和共核附着法检测重叠蛋白质复合物。","authors":"Wenkang Wang, Xiangmao Meng, Ju Xiang, Hayat Dino Bedru, Min Li","doi":"10.1109/TCBB.2024.3429546","DOIUrl":null,"url":null,"abstract":"<p><p>Identification of protein complex is an important issue in the field of system biology, which is crucial to understanding the cellular organization and inferring protein functions. Recently, many computational methods have been proposed to detect protein complexes from protein-protein interaction (PPI) networks. However, most of these methods only focus on local information of proteins in the PPI network, which are easily affected by the noise in the PPI network. Meanwhile, it's still challenging to detect protein complexes, especially for overlapping cases. To address these issues, we propose a new method, named Dopcc, to detect overlapping protein complexes by constructing a multi-metrics network according to different strategies. First, we adopt the Jaccard coefficient to measure the neighbor similarity between proteins and denoise the PPI network. Then, we propose a new strategy, integrating hierarchical compressing with network embedding, to capture the high-order structural similarity between proteins. Further, a new co-core attachment strategy is proposed to detect overlapping protein complexes from multi-metrics. The experimental results show that our proposed method, Dopcc, outperforms the other eight state-of-the-art methods in terms of F-measure, MMR, and Composite Score on two yeast datasets. The source code and datasets can be downloaded from https://github.com/CSUBioGroup/Dopcc.</p>","PeriodicalId":13344,"journal":{"name":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","volume":null,"pages":null},"PeriodicalIF":3.6000,"publicationDate":"2024-07-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dopcc: Detecting overlapping protein complexes via multi-metrics and co-core attachment method.\",\"authors\":\"Wenkang Wang, Xiangmao Meng, Ju Xiang, Hayat Dino Bedru, Min Li\",\"doi\":\"10.1109/TCBB.2024.3429546\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Identification of protein complex is an important issue in the field of system biology, which is crucial to understanding the cellular organization and inferring protein functions. Recently, many computational methods have been proposed to detect protein complexes from protein-protein interaction (PPI) networks. However, most of these methods only focus on local information of proteins in the PPI network, which are easily affected by the noise in the PPI network. Meanwhile, it's still challenging to detect protein complexes, especially for overlapping cases. To address these issues, we propose a new method, named Dopcc, to detect overlapping protein complexes by constructing a multi-metrics network according to different strategies. First, we adopt the Jaccard coefficient to measure the neighbor similarity between proteins and denoise the PPI network. Then, we propose a new strategy, integrating hierarchical compressing with network embedding, to capture the high-order structural similarity between proteins. Further, a new co-core attachment strategy is proposed to detect overlapping protein complexes from multi-metrics. The experimental results show that our proposed method, Dopcc, outperforms the other eight state-of-the-art methods in terms of F-measure, MMR, and Composite Score on two yeast datasets. The source code and datasets can be downloaded from https://github.com/CSUBioGroup/Dopcc.</p>\",\"PeriodicalId\":13344,\"journal\":{\"name\":\"IEEE/ACM Transactions on Computational Biology and Bioinformatics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.6000,\"publicationDate\":\"2024-07-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IEEE/ACM Transactions on Computational Biology and Bioinformatics\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://doi.org/10.1109/TCBB.2024.3429546\",\"RegionNum\":3,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE/ACM Transactions on Computational Biology and Bioinformatics","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1109/TCBB.2024.3429546","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
引用次数: 0

摘要

蛋白质复合物的鉴定是系统生物学领域的一个重要问题,对于理解细胞组织和推断蛋白质功能至关重要。最近,人们提出了许多计算方法来从蛋白质-蛋白质相互作用(PPI)网络中检测蛋白质复合物。然而,这些方法大多只关注 PPI 网络中蛋白质的局部信息,容易受到 PPI 网络中噪声的影响。同时,检测蛋白质复合物仍具有挑战性,尤其是重叠情况。针对这些问题,我们提出了一种名为 Dopcc 的新方法,根据不同的策略构建多度量网络,从而检测重叠的蛋白质复合物。首先,我们采用 Jaccard 系数来测量蛋白质之间的邻接相似性,并对 PPI 网络进行去噪处理。然后,我们提出了一种新策略,将分层压缩与网络嵌入相结合,以捕捉蛋白质之间的高阶结构相似性。此外,我们还提出了一种新的共核附着策略,以从多指标中检测重叠的蛋白质复合物。实验结果表明,在两个酵母数据集上,我们提出的 Dopcc 方法在 F-measure、MMR 和 Composite Score 方面优于其他八种最先进的方法。源代码和数据集可从 https://github.com/CSUBioGroup/Dopcc 下载。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dopcc: Detecting overlapping protein complexes via multi-metrics and co-core attachment method.

Identification of protein complex is an important issue in the field of system biology, which is crucial to understanding the cellular organization and inferring protein functions. Recently, many computational methods have been proposed to detect protein complexes from protein-protein interaction (PPI) networks. However, most of these methods only focus on local information of proteins in the PPI network, which are easily affected by the noise in the PPI network. Meanwhile, it's still challenging to detect protein complexes, especially for overlapping cases. To address these issues, we propose a new method, named Dopcc, to detect overlapping protein complexes by constructing a multi-metrics network according to different strategies. First, we adopt the Jaccard coefficient to measure the neighbor similarity between proteins and denoise the PPI network. Then, we propose a new strategy, integrating hierarchical compressing with network embedding, to capture the high-order structural similarity between proteins. Further, a new co-core attachment strategy is proposed to detect overlapping protein complexes from multi-metrics. The experimental results show that our proposed method, Dopcc, outperforms the other eight state-of-the-art methods in terms of F-measure, MMR, and Composite Score on two yeast datasets. The source code and datasets can be downloaded from https://github.com/CSUBioGroup/Dopcc.

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
CiteScore
7.50
自引率
6.70%
发文量
479
审稿时长
3 months
期刊介绍: IEEE/ACM Transactions on Computational Biology and Bioinformatics emphasizes the algorithmic, mathematical, statistical and computational methods that are central in bioinformatics and computational biology; the development and testing of effective computer programs in bioinformatics; the development of biological databases; and important biological results that are obtained from the use of these methods, programs and databases; the emerging field of Systems Biology, where many forms of data are used to create a computer-based model of a complex biological system
×
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:481959085
Book学术官方微信