De Preter Katleen, Barriot Roland, Speleman Frank, Vandesompele Jo, Moreau Yves
Center for Medical Genetics, Ghent University Hospital, De Pintelaan 185, B-9000 Ghent, Belgium.
Nucleic Acids Res. 2008 Apr;36(7):e43. doi: 10.1093/nar/gkn114. Epub 2008 Mar 16.
The search for feature enrichment is a widely used method to characterize a set of genes. While several tools have been designed for nominal features such as Gene Ontology annotations or KEGG Pathways, very little has been proposed to tackle numerical features such as the chromosomal positions of genes. For instance, microarray studies typically generate gene lists that are differentially expressed in the sample subgroups under investigation, and when studying diseases caused by genome alterations, it is of great interest to delineate the chromosomal regions that are significantly enriched in these lists. In this article, we present a positional gene enrichment analysis method (PGE) for the identification of chromosomal regions that are significantly enriched in a given set of genes. The strength of our method relies on an original query optimization approach that allows to virtually consider all the possible chromosomal regions for enrichment, and on the multiple testing correction which discriminates truly enriched regions versus those that can occur by chance. We have developed a Web tool implementing this method applied to the human genome (http://www.esat.kuleuven.be/~bioiuser/pge). We validated PGE on published lists of differentially expressed genes. These analyses showed significant overrepresentation of known aberrant chromosomal regions.
寻找特征富集是一种广泛用于描述一组基因特征的方法。虽然已经设计了几种工具来处理名义特征,如基因本体注释或KEGG通路,但针对数值特征(如基因的染色体位置)的方法却很少。例如,微阵列研究通常会生成在正在研究的样本亚组中差异表达的基因列表,而在研究由基因组改变引起的疾病时,描绘这些列表中显著富集的染色体区域非常重要。在本文中,我们提出了一种位置基因富集分析方法(PGE),用于识别在给定的一组基因中显著富集的染色体区域。我们方法的优势在于一种原始的查询优化方法,该方法允许虚拟地考虑所有可能的富集染色体区域,以及多重检验校正,它可以区分真正富集的区域和那些可能偶然出现的区域。我们开发了一个网络工具来实现这种应用于人类基因组的方法(http://www.esat.kuleuven.be/~bioiuser/pge)。我们在已发表的差异表达基因列表上验证了PGE。这些分析表明已知异常染色体区域存在显著的过度富集。