Abstract
The rapid accumulation of gene expression data has offered unprecedented opportunities to study human diseases. The National Center for Biotechnology Information Gene Expression Omnibus is currently the largest database that systematically documents the genome-wide molecular basis of diseases. However, thus far, this resource has been far from fully utilized. This paper describes the first study to transform public gene expression repositories into an automated disease diagnosis database. Particularly, we have developed a systematic framework, including a two-stage Bayesian learning approach, to achieve the diagnosis of one or multiple diseases for a query expression profile along a hierarchical disease taxonomy. Our approach, including standardizing cross-platform gene expression data and heterogeneous disease annotations, allows analyzing both sources of information in a unified probabilistic system. A high level of overall diagnostic accuracy was shown by cross validation. It was also demonstrated that the power of our method can increase significantly with the continued growth of public gene expression repositories. Finally, we showed how our disease diagnosis system can be used to characterize complex phenotypes and to construct a disease-drug connectivity map.
MeSH Terms
Access to Information
Algorithms
Artificial Intelligence
Bayes Theorem
Computational Biology/methods
Databases, Factual
Databases, Genetic
Gene Expression Profiling/methods
Genomics/methods
Humans
Information Storage and Retrieval
Oligonucleotide Array Sequence Analysis
Pattern Recognition, Automated/methods
Regression Analysis
Software
User-Computer Interface
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Huang Haiyan
Department of Statistics, University of California, Berkeley, CA 94720, USA. hhuang@stat.berkeley.edu
Liu Chun-Chi
Zhou Xianghong Jasmine
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