由密度距离和头脑风暴过程启发的一种新的识别时间蛋白复合物策略

Xianjun Shen, Jin Zhou, Xingpeng Jiang, Xiaohua Hu, Tingting He, Jincai Yang, Dan Xie
{"title":"由密度距离和头脑风暴过程启发的一种新的识别时间蛋白复合物策略","authors":"Xianjun Shen, Jin Zhou, Xingpeng Jiang, Xiaohua Hu, Tingting He, Jincai Yang, Dan Xie","doi":"10.1109/BIBM.2016.7822701","DOIUrl":null,"url":null,"abstract":"Detection of protein complexes and functional modules plays a crucial role for strengthening the comprehension of cellular organization and biological functions on the dynamic protein-protein interaction network. In this article, we put forward a new strategy to identify temporal protein complexes. Integrating time-course gene expression data into static protein interaction data, a series of time-sequenced subnetworks were constructed. Then we combined the network topology and gene ontology information for defining the distance between proteins in PPI network. A novel method to find the cluster centers and then form initial clusters was based on the idea that cluster centers are usually recognized as nodes with higher densities than their neighbors and with a relatively larger distance from other cluster centers. Finally, inspired by the brainstorming discussion process, two ways are introduced to update the initial clusters for achieving the optimal results. After the filtering and merging procedure, experimental results demonstrated that the proposed strategy had a good performance comparing with the other four advanced algorithms - MCODE, FAG-EC, HC-PIN, and CNC.","PeriodicalId":345384,"journal":{"name":"2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","volume":"2 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2016-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"A novel identified temporal protein complexes strategy inspired by density-distance and brainstorming process\",\"authors\":\"Xianjun Shen, Jin Zhou, Xingpeng Jiang, Xiaohua Hu, Tingting He, Jincai Yang, Dan Xie\",\"doi\":\"10.1109/BIBM.2016.7822701\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Detection of protein complexes and functional modules plays a crucial role for strengthening the comprehension of cellular organization and biological functions on the dynamic protein-protein interaction network. In this article, we put forward a new strategy to identify temporal protein complexes. Integrating time-course gene expression data into static protein interaction data, a series of time-sequenced subnetworks were constructed. Then we combined the network topology and gene ontology information for defining the distance between proteins in PPI network. A novel method to find the cluster centers and then form initial clusters was based on the idea that cluster centers are usually recognized as nodes with higher densities than their neighbors and with a relatively larger distance from other cluster centers. Finally, inspired by the brainstorming discussion process, two ways are introduced to update the initial clusters for achieving the optimal results. After the filtering and merging procedure, experimental results demonstrated that the proposed strategy had a good performance comparing with the other four advanced algorithms - MCODE, FAG-EC, HC-PIN, and CNC.\",\"PeriodicalId\":345384,\"journal\":{\"name\":\"2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)\",\"volume\":\"2 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-12-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1109/BIBM.2016.7822701\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"2016 IEEE International Conference on Bioinformatics and Biomedicine (BIBM)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1109/BIBM.2016.7822701","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 2

摘要

蛋白质复合物和功能模块的检测对于加强对蛋白质-蛋白质动态相互作用网络中细胞组织和生物功能的理解起着至关重要的作用。在本文中,我们提出了一种新的识别颞叶蛋白复合物的策略。将时序基因表达数据整合到静态蛋白相互作用数据中,构建了一系列时序子网络。然后结合网络拓扑和基因本体信息来定义PPI网络中蛋白质之间的距离。基于集群中心通常被识别为密度高于相邻节点且与其他集群中心距离相对较大的节点,提出了一种寻找集群中心并形成初始集群的新方法。最后,受头脑风暴讨论过程的启发,引入了两种方法来更新初始聚类以获得最佳结果。经过滤波和合并后的实验结果表明,与MCODE、FAG-EC、HC-PIN和CNC等四种先进算法相比,该策略具有良好的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel identified temporal protein complexes strategy inspired by density-distance and brainstorming process
Detection of protein complexes and functional modules plays a crucial role for strengthening the comprehension of cellular organization and biological functions on the dynamic protein-protein interaction network. In this article, we put forward a new strategy to identify temporal protein complexes. Integrating time-course gene expression data into static protein interaction data, a series of time-sequenced subnetworks were constructed. Then we combined the network topology and gene ontology information for defining the distance between proteins in PPI network. A novel method to find the cluster centers and then form initial clusters was based on the idea that cluster centers are usually recognized as nodes with higher densities than their neighbors and with a relatively larger distance from other cluster centers. Finally, inspired by the brainstorming discussion process, two ways are introduced to update the initial clusters for achieving the optimal results. After the filtering and merging procedure, experimental results demonstrated that the proposed strategy had a good performance comparing with the other four advanced algorithms - MCODE, FAG-EC, HC-PIN, and CNC.
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
自引率
0.00%
发文量
0
×
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