Evidence map›Paper›PMID 30241459›Full record

ArticleBMC bioinformatics2018

Identifying protein complexes based on node embeddings obtained from protein-protein interaction networks.

Xiaoxia Liu, Zhihao Yang, Shengtian Sang, Ziwei Zhou, Lei Wang, Yin Zhang, Hongfei Lin, Jian Wang, Bo Xu

Open access · goldAbstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 39% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

4 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Heterogeneous network approaches to protein pathway prediction.Computational and structural biotechnology journal · 2024
    Review
  3. Article
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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

9 authors at 1 institution in 1 country.

Xiaoxia LiuCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Zhihao YangCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China. yangzh@dlut.edu.cn.
Shengtian SangCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Ziwei ZhouCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Lei WangBeijing Institute of Health Administration and Medical Information, Beijing, 100850, People's Republic of China. wangleibihami@gmail.com.
Yin ZhangBeijing Institute of Health Administration and Medical Information, Beijing, 100850, People's Republic of China.
Hongfei LinCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Jian WangCollege of Computer Science and Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Bo XuSchool of Software Technology, Dalian University of Technology, Dalian, 116024, Liaoning, People's Republic of China.
Dalian University of Technology · CN

Funding

National Key Research and Development Program of China 2016YFC0901902National Natural Science Foundation of China 61272373National Natural Science Foundation of China 61572098National Natural Science Foundation of China 61572102National Natural Science Foundation of China (CN) 61572098Trans-Century Training Program Foundation for the Talents by the Ministry of Education of China NCET-13-0084
6 · The paper itself

Abstract

backgroundProtein complexes are one of the keys to deciphering the behavior of a cell system. During the past decade, most computational approaches used to identify protein complexes have been based on discovering densely connected subgraphs in protein-protein interaction (PPI) networks. However, many true complexes are not dense subgraphs and these approaches show limited performances for detecting protein complexes from PPI networks.

resultsTo solve these problems, in this paper we propose a supervised learning method based on network node embeddings which utilizes the informative properties of known complexes to guide the search process for new protein complexes. First, node embeddings are obtained from human protein interaction network. Then the protein interactions are weighted through the similarities between node embeddings. After that, the supervised learning method is used to detect protein complexes. Then the random forest model is used to filter the candidate complexes in order to obtain the final predicted complexes. Experimental results on real human and yeast protein interaction networks show that our method effectively improves the performance for protein complex detection.

conclusionsWe provided a new method for identifying protein complexes from human and yeast protein interaction networks, which has great potential to benefit the field of protein complex detection.

Indexed as

AlgorithmsProtein Interaction MapsComputational BiologyHumansProtein Interaction MappingSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSaccharomyces cerevisiae ProteinsNode embeddingsProtein complex detectionRandom forestSupervised learning method

Identifiers

PMID30241459
PMCPMC6150962
OpenAlexW2889626364

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.