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CTGR-Span: Efficient mining of cross-timepoint gene regulation sequential patterns from microarray datasets

机译:CTGR-Span:从微阵列数据集中高效挖掘跨时间点基因调控的顺序模式

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Sequential pattern mining techniques have been widely used in different topics of interest, such as mining customer purchasing sequences from a transactional database. Notably, observation of gene expressions to discover gene regulations during biological or clinical progression via microarray approaches has become the dominant trend. By converting microarray datasets into the format of transactional databases, sequential patterns implying gene regulations could be identified. However, there exists no effective method in current studies that can handle such kind of dataset as every transaction may contain too many items/genes and the resultant patterns are very susceptible to item order. We propose a new method called CTGR-Span (Cross-Timepoint Gene Regulation Sequential Patterns) to efficiently mine CTGR-SPs (cross-timepoint gene regulation sequential patterns). The proposed method was experimented with two publicly available human time course microarray datasets and it outperformed traditional methods over 2,000 times in terms of the execution efficiency. Furthermore, via a Gene Ontology enrichment analysis, the resultant patterns are more meaningful biologically compared to previous literature reports. Hence, it could provide biologists more insights into the mechanisms of novel gene regulations in certain disease progressions.
机译:顺序模式挖掘技术已广泛用于感兴趣的不同主题,例如从事务数据库中挖掘客户购买序列。值得注意的是,通过微阵列方法观察基因表达以发现生物学或临床进展过程中的基因调控已成为主要趋势。通过将微阵列数据集转换为交易数据库的格式,可以识别出暗示基因调控的顺序模式。但是,当前的研究中没有有效的方法可以处理此类数据集,因为每个事务可能包含太多的项目/基因,并且产生的模式非常容易受到项目顺序的影响。我们提出了一种称为CTGR-Span(跨时间点基因调节顺序模式)的新方法,以有效地挖掘CTGR-SP(跨时间点基因调节顺序模式)。该方法在两个公开的人类时间过程微阵列数据集上进行了实验,在执行效率方面比传统方法高出2000倍。此外,通过基因本体论富集分析,与以前的文献报道相比,所得模式在生物学上更有意义。因此,它可以为生物学家提供更多有关某些疾病进展中新基因调控机制的见解。

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