Watkinson John, Liang Kuo-Ching, Wang Xiadong, Zheng Tian, Anastassiou Dimitris
Department of Electrical Engineering.
Ann N Y Acad Sci. 2009 Mar;1158:302-13. doi: 10.1111/j.1749-6632.2008.03757.x.
This paper describes the technique designated best performer in the 2nd conference on Dialogue for Reverse Engineering Assessments and Methods (DREAM2) Challenge 5 (unsigned genome-scale network prediction from blinded microarray data). Existing algorithms use the pairwise correlations of the expression levels of genes, which provide valuable but insufficient information for the inference of regulatory interactions. Here we present a computational approach based on the recently developed context likelihood of related (CLR) algorithm, extracting additional complementary information using the information theoretic measure of synergy and assigning a score to each ordered pair of genes measuring the degree of confidence that the first gene regulates the second. When tested on a set of publicly available Escherichia coli gene-expression data with known assumed ground truth, the synergy augmented CLR (SA-CLR) algorithm had significantly improved prediction performance when compared to CLR. There is also enhanced potential for biological discovery as a result of the identification of the most likely synergistic partner genes involved in the interactions.
本文描述了在第二届逆向工程评估与方法对话会议(DREAM2)挑战赛5(从盲法微阵列数据进行无符号基因组规模网络预测)中表现最佳的技术。现有算法使用基因表达水平的成对相关性,这为推断调控相互作用提供了有价值但不充分的信息。在此,我们提出一种基于最近开发的相关上下文似然性(CLR)算法的计算方法,利用协同作用的信息理论度量提取额外的互补信息,并为每对有序基因赋予一个分数,以衡量第一个基因调控第二个基因的置信程度。当在一组具有已知假定真实情况的公开可用大肠杆菌基因表达数据上进行测试时,与CLR相比,协同增强CLR(SA-CLR)算法的预测性能有显著提高。由于识别出了相互作用中最可能的协同伙伴基因,生物发现的潜力也得到了增强。