4.7 Article

idenPC-MIIP: identify protein complexes from weighted PPI networks using mutual important interacting partner relation

期刊

BRIEFINGS IN BIOINFORMATICS
卷 22, 期 2, 页码 1972-1983

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bib/bbaa016

关键词

protein complexes; protein-protein interaction networks; mutual important interacting partner relation

资金

  1. Beijing Natural Science Foundation [JQ19019]
  2. National Natural Science Foundation of China [61672184, 61822306]
  3. Fok Ying-Tung Education Foundation for Young Teachers in the Higher Education Institutions of China [161063]
  4. Scientific Research Foundation in Shenzhen [JCYJ20180306172207178]

向作者/读者索取更多资源

Protein complexes are key units for studying a cell system, and high-throughput approaches have enabled the determination of PPI data. The proposed mutual important interacting partner relation and the new algorithm idenPC-MIIP show improved performance in identifying protein complexes compared to existing methods.
Protein complexes are key units for studying a cell system. During the past decades, the genome-scale protein-protein interaction (PPI) data have been determined by high-throughput approaches, which enables the identification of protein complexes from PPI networks. However, the high-throughput approaches often produce considerable fraction of false positive and negative samples. In this study, we propose the mutual important interacting partner relation to reflect the co-complex relationship of two proteins based on their interaction neighborhoods. In addition, a new algorithm called idenPC-MIIP is developed to identify protein complexes from weighted PPI networks. The experimental results on two widely used datasets show that idenPC-MIIP outperforms 17 state-of-the-art methods, especially for identification of small protein complexes with only two or three proteins.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据