Nakahara Hiroyuki, Nishimura Shin-ichi, Inoue Masato, Hori Gen, Amari Shun-ichi
Lab. for Mathematical Neuroscience, RIKEN Brain Science Institute, Saitama 351-0198, Japan.
Bioinformatics. 2003 Jun 12;19(9):1124-31. doi: 10.1093/bioinformatics/btg098.
Given the vast amount of gene expression data, it is essential to develop a simple and reliable method of investigating the fine structure of gene interaction. We show how an information geometric measure achieves this.
We introduce an information geometric measure of binary random vectors and show how this measure reveals the fine structure of gene interaction. In particular, we propose an iterative procedure by using this measure (called IPIG). The procedure finds higher-order dependencies which may underlie the interaction between two genes of interest. To demonstrate the method, we investigate the interaction between the two genes of interest in the data from human acute lymphoblastic leukemia cells. The method successfully discovered biologically known findings and also selected other genes as hidden causes that constitute the interaction.
Softwares are currently not available but are possibly made available in future at http://www.mns.brain.riken.go.jp/~nakahara/DNA_pub.html where all the related information is also linked.
鉴于大量的基因表达数据,开发一种简单可靠的方法来研究基因相互作用的精细结构至关重要。我们展示了一种信息几何度量是如何实现这一点的。
我们引入了二元随机向量的信息几何度量,并展示了该度量如何揭示基因相互作用的精细结构。特别是,我们提出了一种使用此度量的迭代程序(称为IPIG)。该程序发现了可能是两个感兴趣基因之间相互作用基础的高阶依赖性。为了演示该方法,我们研究了来自人类急性淋巴细胞白血病细胞数据中两个感兴趣基因之间的相互作用。该方法成功发现了生物学上已知的发现,还选择了其他基因作为构成相互作用的隐藏原因。
目前没有软件,但未来可能会在http://www.mns.brain.riken.go.jp/~nakahara/DNA_pub.html上提供,所有相关信息也链接在该网站上。