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Time-series RNA-seq analysis package (TRAP) and its application to the analysis of rice, Oryza sativa L. ssp. Japonica, upon drought stress

机译:时间序列RNA序列分析软件包(TRAP)及其在水稻Oryza sativa L. ssp。干旱胁迫下的粳稻

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摘要

Measuring expression levels of genes at the whole genome level can be useful for many purposes, especially for revealing biological pathways underlying specific phenotype conditions. When gene expression is measured over a time period, we have opportunities to understand how organisms react to stress conditions over time. Thus many biologists routinely measure whole genome level gene expressions at multiple time points. However, there are several technical difficulties for analyzing such whole genome expression data. In addition, these days gene expression data is often measured by using RNA-sequencing rather than microarray technologies and then analysis of expression data is much more complicated since the analysis process should start with mapping short reads and produce differentially activated pathways and also possibly interactions among pathways. In addition, many useful tools for analyzing microarray gene expression data are not applicable for the RNA-seq data. Thus a comprehensive package for analyzing time series transcriptome data is much needed. In this article, we present a comprehensive package, Time-series RNA-seq Analysis Package (TRAP), integrating all necessary tasks such as mapping short reads, measuring gene expression levels, finding differentially expressed genes (DEGs), clustering and pathway analysis for time-series data in a single environment. In addition to implementing useful algorithms that are not available for RNA-seq data, we extended existing pathway analysis methods, ORA and SPIA, for time series analysis and estimates statistical values for combined dataset by an advanced metric. TRAP also produces visual summary of pathway interactions. Gene expression change labeling, a practical clustering method used in TRAP, enables more accurate interpretation of the data when combined with pathway analysis. We applied our methods on a real dataset for the analysis of rice (Oryza sativa L. Japonica nipponbare) upon drought stress. The result showed that TRAP was able to detect pathways more accurately than several existing methods. TRAP is available at http://biohealth.snu.ac.kr/software/TRAP/.
机译:在整个基因组水平上测量基因的表达水平可用于许多目的,尤其是对于揭示特定表型条件下的生物学途径。在一段时间内测量基因表达时,我们就有机会了解生物体如何随时间变化应对压力条件。因此,许多生物学家常规地在多个时间点测量整个基因组水平的基因表达。但是,分析这种全基因组表达数据存在若干技术困难。此外,这些天的基因表达数据通常是使用RNA测序而不是微阵列技术来测量的,因此表达数据的分析要复杂得多,因为分析过程应从绘制短读段开始,并产生差异激活的途径,以及可能的相互作用。途径。此外,用于分析微阵列基因表达数据的许多有用工具不适用于RNA-seq数据。因此,非常需要用于分析时间序列转录组数据的综合软件包。在本文中,我们提供了一个全面的程序包,即时间序列RNA序列分析程序包(TRAP),该程序包集成了所有必需的任务,例如绘制短读图,测量基因表达水平,寻找差异表达基因(DEG),聚类和途径分析单个环境中的时间序列数据。除了实施不适用于RNA序列数据的有用算法之外,我们还扩展了现有的路径分析方法ORA和SPIA,用于时间序列分析,并通过高级度量来估计组合数据集的统计值。 TRAP还可以生成途径相互作用的直观摘要。基因表达变化标签是TRAP中使用的一种实用的聚类方法,当与途径分析结合使用时,可以更准确地解释数据。我们将我们的方法应用于真实数据集,以分析干旱胁迫下的水稻(Oryza sativa L. Japonica nipponbare)。结果表明,TRAP比几种现有方法能够更准确地检测途径。可从http://biohealth.snu.ac.kr/software/TRAP/获得TRAP。

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