Evidence map›Paper›PMID 26634213›Full record

ArticleBioMed research international2015

Using Weighted Sparse Representation Model Combined with Discrete Cosine Transformation to Predict Protein-Protein Interactions from Protein Sequence.

Yu-An Huang, Zhu-Hong You, Xin Gao, Leon Wong, Lirong Wang

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Article in BioMed research international, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

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0cells of the map it votes in
52citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

52 citing papers in PubMed.

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  11. Improved global protein homolog detection with major gains in function identification.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  12. ProtInteract: A deep learning framework for predicting protein-protein interactions.Computational and structural biotechnology journal · 2023
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  13. Review
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Yu-An HuangCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Zhu-Hong YouSchool of Computer Science and Technology, China University of Mining and Technology, Xuzhou, Jiangsu 221116, China.
Xin GaoDepartment of Medical Imaging, Suzhou Institute of Biomedical Engineering and Technology, Suzhou, Jiangsu 215163, China.
Leon WongCollege of Computer Science and Software Engineering, Shenzhen University, Shenzhen, Guangdong 518060, China.
Lirong WangSchool of Electronic and Information Engineering, Soochow University, Suzhou, Jiangsu 215123, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Increasing demand for the knowledge about protein-protein interactions (PPIs) is promoting the development of methods for predicting protein interaction network. Although high-throughput technologies have generated considerable PPIs data for various organisms, it has inevitable drawbacks such as high cost, time consumption, and inherently high false positive rate. For this reason, computational methods are drawing more and more attention for predicting PPIs. In this study, we report a computational method for predicting PPIs using the information of protein sequences. The main improvements come from adopting a novel protein sequence representation by using discrete cosine transform (DCT) on substitution matrix representation (SMR) and from using weighted sparse representation based classifier (WSRC). When performing on the PPIs dataset of Yeast, Human, and H. pylori, we got excellent results with average accuracies as high as 96.28%, 96.30%, and 86.74%, respectively, significantly better than previous methods. Promising results obtained have proven that the proposed method is feasible, robust, and powerful. To further evaluate the proposed method, we compared it with the state-of-the-art support vector machine (SVM) classifier. Extensive experiments were also performed in which we used Yeast PPIs samples as training set to predict PPIs of other five species datasets.

Indexed as

Models, ChemicalAmino Acid SequenceBinding SitesMolecular Docking SimulationMolecular Sequence DataProtein BindingProtein Interaction MappingSaccharomyces cerevisiae ProteinsSequence AlignmentSequence Analysis, ProteinSaccharomyces cerevisiae Proteins

Identifiers

PMID26634213
PMCPMC4641304

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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.