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Enrichment constrained time-dependent clustering analysis for finding meaningful temporal transcription modules

机译:富集约束时间相关的聚类分析,用于寻找有意义的时间转录模块

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MOTIVATION: Clustering is a popular data exploration technique widely used in microarray data analysis. When dealing with time-series data, most conventional clustering algorithms, however, either use one-way clustering methods, which fail to consider the heterogeneity of temporary domain, or use two-way clustering methods that do not take into account the time dependency between samples, thus producing less informative results. Furthermore, enrichment analysis is often performed independent of and after clustering and such practice, though capable of revealing biological significant clusters, cannot guide the clustering to produce biologically significant result. RESULT: We present a new enrichment constrained framework (ECF) coupled with a time-dependent iterative signature algorithm (TDISA), which, by applying a sliding time window to incorporate the time dependency of samples and imposing an enrichment constraint to parameters of clustering, allows supervised identification of temporal transcription modules (TTMs) that are biologically meaningful. Rigorous mathematical definitions of TTM as well as the enrichment constraint framework are also provided that serve as objective functions for retrieving biologically significant modules. We applied the enrichment constrained time-dependent iterative signature algorithm (ECTDISA) to human gene expression time-series data of Kaposi's sarcoma-associated herpesvirus (KSHV) infection of human primary endothelial cells; the result not only confirms known biological facts, but also reveals new insight into the molecular mechanism of KSHV infection. AVAILABILITY: Data and Matlab code are available at http://engineering.utsa.edu/ approximately yfhuang/ECTDISA.html. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
机译:动机:聚类是一种流行的数据探索技术,广泛用于微阵列数据分析中。但是,在处理时间序列数据时,大多数传统的聚类算法要么使用单向聚类方法(无法考虑临时域的异构性),要么使用不考虑时间之间的时间依赖性的双向聚类方法。样本,因此产生的信息量较少。此外,富集分析通常独立于聚类和在聚类之后进行,尽管这种实践能够揭示生物学上的重要簇,但不能指导聚类产生生物学上的重要结果。结果:我们提出了一种新的富集约束框架(ECF),并结合了时间相关的迭代签名算法(TDISA),该算法通过应用滑动时间窗合并样本的时间依赖性并将富集约束施加到聚类参数上,可以监督地识别具有生物学意义的暂时转录模块(TTM)。还提供了TTM的严格数学定义以及富集约束框架,它们充当了检索具有生物学意义的模块的目标功能。我们将富集受限时间依赖的迭代签名算法(ECTDISA)应用于人类原代内皮细胞的卡波西氏肉瘤相关疱疹病毒(KSHV)感染的人类基因表达时间序列数据;结果不仅证实了已知的生物学事实,而且揭示了对KSHV感染分子机制的新见解。可用性:数据和Matlab代码可在http://engineering.utsa.edu/大约yfhuang / ECTDISA.html上获得。补充信息:补充数据可从Bioinformatics在线获得。

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