Nacu Serban, Critchley-Thorne Rebecca, Lee Peter, Holmes Susan
Department of Statistics, Stanford University, Stanford, CA 94305, USA.
Bioinformatics. 2007 Apr 1;23(7):850-8. doi: 10.1093/bioinformatics/btm019. Epub 2007 Jan 31.
We address the problem of using expression data and prior biological knowledge to identify differentially expressed pathways or groups of genes. Following an idea of Ideker et al. (2002), we construct a gene interaction network and search for high-scoring subnetworks. We make several improvements in terms of scoring functions and algorithms, resulting in higher speed and accuracy and easier biological interpretation. We also assign significance levels to our results, adjusted for multiple testing. Our methods are successfully applied to three human microarray data sets, related to cancer and the immune system, retrieving several known and potential pathways. The method, denoted by the acronym GXNA (Gene eXpression Network Analysis) is implemented in software that is publicly available and can be used on virtually any microarray data set.
The source code and executable for the software, as well as certain supplemental materials, can be downloaded from http://stat.stanford.edu/~serban/gxna.
我们解决了利用表达数据和先验生物学知识来识别差异表达的通路或基因群组的问题。遵循艾德克等人(2002年)的思路,我们构建了一个基因相互作用网络并搜索高分子网。我们在评分函数和算法方面做了多项改进,从而提高了速度和准确性,并使生物学解释更加容易。我们还为结果赋予了显著性水平,并针对多重检验进行了调整。我们的方法成功应用于三个与癌症和免疫系统相关的人类微阵列数据集,检索到了几条已知和潜在的通路。该方法简称为GXNA(基因表达网络分析),已在公开可用的软件中实现,几乎可用于任何微阵列数据集。
该软件的源代码和可执行文件,以及某些补充材料,可从http://stat.stanford.edu/~serban/gxna下载。