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Constructing an integrated gene similarity network for the identification of disease genes

Overview of attention for article published in Journal of Biomedical Semantics, September 2017
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Title
Constructing an integrated gene similarity network for the identification of disease genes
Published in
Journal of Biomedical Semantics, September 2017
DOI 10.1186/s13326-017-0141-1
Pubmed ID
Authors

Zhen Tian, Maozu Guo, Chunyu Wang, LinLin Xing, Lei Wang, Yin Zhang

Abstract

Discovering novel genes that are involved human diseases is a challenging task in biomedical research. In recent years, several computational approaches have been proposed to prioritize candidate disease genes. Most of these methods are mainly based on protein-protein interaction (PPI) networks. However, since these PPI networks contain false positives and only cover less half of known human genes, their reliability and coverage are very low. Therefore, it is highly necessary to fuse multiple genomic data to construct a credible gene similarity network and then infer disease genes on the whole genomic scale. We proposed a novel method, named RWRB, to infer causal genes of interested diseases. First, we construct five individual gene (protein) similarity networks based on multiple genomic data of human genes. Then, an integrated gene similarity network (IGSN) is reconstructed based on similarity network fusion (SNF) method. Finally, we employee the random walk with restart algorithm on the phenotype-gene bilayer network, which combines phenotype similarity network, IGSN as well as phenotype-gene association network, to prioritize candidate disease genes. We investigate the effectiveness of RWRB through leave-one-out cross-validation methods in inferring phenotype-gene relationships. Results show that RWRB is more accurate than state-of-the-art methods on most evaluation metrics. Further analysis shows that the success of RWRB is benefited from IGSN which has a wider coverage and higher reliability comparing with current PPI networks. Moreover, we conduct a comprehensive case study for Alzheimer's disease and predict some novel disease genes that supported by literature. RWRB is an effective and reliable algorithm in prioritizing candidate disease genes on the genomic scale. Software and supplementary information are available at http://nclab.hit.edu.cn/~tianzhen/RWRB/ .

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 33 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 33 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 8 24%
Student > Ph. D. Student 4 12%
Student > Bachelor 3 9%
Student > Doctoral Student 3 9%
Student > Master 2 6%
Other 2 6%
Unknown 11 33%
Readers by discipline Count As %
Biochemistry, Genetics and Molecular Biology 7 21%
Computer Science 4 12%
Pharmacology, Toxicology and Pharmaceutical Science 2 6%
Medicine and Dentistry 2 6%
Nursing and Health Professions 1 3%
Other 4 12%
Unknown 13 39%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 04 January 2018.
All research outputs
#20,458,307
of 23,015,156 outputs
Outputs from Journal of Biomedical Semantics
#335
of 364 outputs
Outputs of similar age
#278,113
of 318,389 outputs
Outputs of similar age from Journal of Biomedical Semantics
#16
of 17 outputs
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So far Altmetric has tracked 364 research outputs from this source. They receive a mean Attention Score of 4.6. This one is in the 1st percentile – i.e., 1% of its peers scored the same or lower than it.
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