A comparison of graph- and kernel-based -omics data integration algorithms for classifying complex traits.
Journal Article (Journal Article)
BACKGROUND: High-throughput sequencing data are widely collected and analyzed in the study of complex diseases in quest of improving human health. Well-studied algorithms mostly deal with single data source, and cannot fully utilize the potential of these multi-omics data sources. In order to provide a holistic understanding of human health and diseases, it is necessary to integrate multiple data sources. Several algorithms have been proposed so far, however, a comprehensive comparison of data integration algorithms for classification of binary traits is currently lacking. RESULTS: In this paper, we focus on two common classes of integration algorithms, graph-based that depict relationships with subjects denoted by nodes and relationships denoted by edges, and kernel-based that can generate a classifier in feature space. Our paper provides a comprehensive comparison of their performance in terms of various measurements of classification accuracy and computation time. Seven different integration algorithms, including graph-based semi-supervised learning, graph sharpening integration, composite association network, Bayesian network, semi-definite programming-support vector machine (SDP-SVM), relevance vector machine (RVM) and Ada-boost relevance vector machine are compared and evaluated with hypertension and two cancer data sets in our study. In general, kernel-based algorithms create more complex models and require longer computation time, but they tend to perform better than graph-based algorithms. The performance of graph-based algorithms has the advantage of being faster computationally. CONCLUSIONS: The empirical results demonstrate that composite association network, relevance vector machine, and Ada-boost RVM are the better performers. We provide recommendations on how to choose an appropriate algorithm for integrating data from multiple sources.
Full Text
Duke Authors
Cited Authors
- Yan, KK; Zhao, H; Pang, H
Published Date
- December 6, 2017
Published In
Volume / Issue
- 18 / 1
Start / End Page
- 539 -
PubMed ID
- 29212468
Pubmed Central ID
- PMC6389230
Electronic International Standard Serial Number (EISSN)
- 1471-2105
Digital Object Identifier (DOI)
- 10.1186/s12859-017-1982-4
Language
- eng
Conference Location
- England