Evidence map›Paper›PMID 25282536›Full record

ArticleBMC bioinformatics2014

Detecting temporal protein complexes from dynamic protein-protein interaction networks.

Le Ou-Yang, Dao-Qing Dai, Xiao-Li Li, Min Wu, Xiao-Fei Zhang, Peng Yang

Abstract read
In one paragraph

Article in BMC bioinformatics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

21 citing papers in PubMed.

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  9. Temporal networks in biology and medicine: a survey on models, algorithms, and tools.Network modeling and analysis in health informatics and bioinformatics · 2023
    Review
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Le Ou-Yang
Dao-Qing DaiIntelligent Data Center and Department of Mathematics, Sun Yat-Sen University, Guangzhou 510275, China. stsddq@mail.sysu.edu.cn.
Xiao-Li Li
Min Wu
Xiao-Fei Zhang
Peng Yang

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProteins dynamically interact with each other to perform their biological functions. The dynamic operations of protein interaction networks (PPI) are also reflected in the dynamic formations of protein complexes. Existing protein complex detection algorithms usually overlook the inherent temporal nature of protein interactions within PPI networks. Systematically analyzing the temporal protein complexes can not only improve the accuracy of protein complex detection, but also strengthen our biological knowledge on the dynamic protein assembly processes for cellular organization.

resultsIn this study, we propose a novel computational method to predict temporal protein complexes. Particularly, we first construct a series of dynamic PPI networks by joint analysis of time-course gene expression data and protein interaction data. Then a Time Smooth Overlapping Complex Detection model (TS-OCD) has been proposed to detect temporal protein complexes from these dynamic PPI networks. TS-OCD can naturally capture the smoothness of networks between consecutive time points and detect overlapping protein complexes at each time point. Finally, a nonnegative matrix factorization based algorithm is introduced to merge those very similar temporal complexes across different time points.

conclusionsExtensive experimental results demonstrate the proposed method is very effective in detecting temporal protein complexes than the state-of-the-art complex detection techniques.

Indexed as

AlgorithmsComputational BiologyGene Expression ProfilingProtein Interaction MappingProteinsTime FactorsProteins

Identifiers

PMID25282536
PMCPMC4288635

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.