Please use this identifier to cite or link to this item: https://doi.org/10.1371/journal.pone.0097079
Title: Ensemble positive unlabeled learning for disease gene identification
Authors: Yang P.
Li X. 
Chua H.-N.
Kwoh C.-K.
Ng S.-K.
Keywords: article
cardiovascular disease
classification algorithm
comparative study
endocrine disease
ensemble positive unlabeled learning
eye disease
gene expression
gene identification
gene ontology
genetic similarity
genotype phenotype correlation
learning algorithm
machine learning
measurement accuracy
metabolic disorder
neoplasm
neurologic disease
prediction
protein interaction
sensitivity analysis
algorithm
artificial intelligence
biological model
biology
evaluation study
gene regulatory network
genetic association
genetic disorder
genetics
human
phenotype
procedures
selection bias
trends
Algorithms
Artificial Intelligence
Computational Biology
Gene Ontology
Gene Regulatory Networks
Genetic Association Studies
Genetic Diseases, Inborn
Humans
Models, Genetic
Phenotype
Selection Bias
Issue Date: 2014
Citation: Yang P., Li X., Chua H.-N., Kwoh C.-K., Ng S.-K. (2014). Ensemble positive unlabeled learning for disease gene identification. PLoS ONE 9 (5) : e97079. ScholarBank@NUS Repository. https://doi.org/10.1371/journal.pone.0097079
Rights: Attribution 4.0 International
Abstract: An increasing number of genes have been experimentally confirmed in recent years as causative genes to various human diseases. The newly available knowledge can be exploited by machine learning methods to discover additional unknown genes that are likely to be associated with diseases. In particular, positive unlabeled learning (PU learning) methods, which require only a positive training set P (confirmed disease genes) and an unlabeled set U (the unknown candidate genes) instead of a negative training set N, have been shown to be effective in uncovering new disease genes in the current scenario. Using only a single source of data for prediction can be susceptible to bias due to incompleteness and noise in the genomic data and a single machine learning predictor prone to bias caused by inherent limitations of individual methods. In this paper, we propose an effective PU learning framework that integrates multiple biological data sources and an ensemble of powerful machine learning classifiers for disease gene identification. Our proposed method integrates data from multiple biological sources for training PU learning classifiers. A novel ensemble-based PU learning method EPU is then used to integrate multiple PU learning classifiers to achieve accurate and robust disease gene predictions. Our evaluation experiments across six disease groups showed that EPU achieved significantly better results compared with various state-of-the-art prediction methods as well as ensemble learning classifiers. Through integrating multiple biological data sources for training and the outputs of an ensemble of PU learning classifiers for prediction, we are able to minimize the potential bias and errors in individual data sources and machine learning algorithms to achieve more accurate and robust disease gene predictions. In the future, our EPU method provides an effective framework to integrate the additional biological and computational resources for better disease gene predictions. © 2014 Yang et al.
Source Title: PLoS ONE
URI: https://scholarbank.nus.edu.sg/handle/10635/161412
ISSN: 1932-6203
DOI: 10.1371/journal.pone.0097079
Rights: Attribution 4.0 International
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