Identification of mitochondrial disease genes through integrative analysis of multiple datasets

被引:8
|
作者
Aiyar, Raeka S. [1 ]
Gagneur, Julien [1 ]
Steinmetz, Lars M. [1 ]
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
关键词
Functional genomics; Mitochondria; Genetic disorder; Genome-wide dataset; Discrimination analysis; Positional cloning; Functional gene network; Machine learning; Bayesian data integration; Support vector machine;
D O I
10.1016/j.ymeth.2008.10.002
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Determining the genetic factors in a disease is crucial to elucidating its molecular basis. This task is challenging due to a lack of information on gene function. The integration of large-scale functional genomics data has proven to be an effective strategy to prioritize candidate disease genes. Mitochondrial disorders are a prevalent and heterogeneous class of diseases that are particularly amenable to this approach. Here we explain the application of integrative approaches to the identification of mitochondrial disease genes. We first examine various datasets that can be used to evaluate the involvement of each gene in mitochondrial function. The data integration methodology is then described, accompanied by examples of common implementations. Finally, we discuss how gene networks are constructed using integrative techniques and applied to candidate gene prioritization. Relevant public data resources are indicated. This report highlights the success and potential of data integration as well as its applicability to the search for mitochondrial disease genes. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:248 / 255
页数:8
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