首页> 外文期刊>Methods: A Companion to Methods in Enzymology >Time-series RNA-seq analysis package (TRAP) and its application to the analysis of rice, Oryza sativa L. ssp. Japonica, upon drought stress
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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-SEQ分析包(陷阱)及其在水稻分析中的应用,ORYZA Sativa L. SSP。 粳稻,干旱压力

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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:在全基因组水平下测量基因的表达水平可用于许多目的,特别是用于揭示特定表型条件下面的生物途径。当在一段时间内测量基因表达时,我们有机会了解有机体如何随着时间的推移而对压力的影响。因此,许多生物学家在多个时间点常规测量全基因组水平基因表达。然而,用于分析这种全基因组表达数据存在若干技术难题。此外,这些天基因表达数据通常通过使用RNA测序而不是微阵列技术来测量,然后表达数据的分析更加复杂,因为分析过程应以映射短读取开始并产生差异激活的途径,并且还可能在相互作用中进行相互作用。途径。此外,许多用于分析微阵列基因表达数据的有用工具不适用于RNA-SEQ数据。因此,需要一个用于分析时间序列转录组数据的全面包。在本文中,我们呈现了一个全面的包,时间序列RNA-SEQ分析包(陷阱),整合所有必要的任务,如映射短读取,测量基因表达水平,发现差异表达基因(DEG),聚类和途径分析单个环境中的时间序列数据。除了实现RNA-SEQ数据不可用的有用算法之外,我们还扩展了现有的途径分析方法,ORA和SPIA,用于时间序列分析,并通过高级度量估算组合数据集的统计值。陷阱还产生途径相互作用的视觉概述。基因表达改变标签,陷阱中使用的实际聚类方法,使得与途径分析结合时,可以更准确地解释数据。我们在真正的数据集上应用了对水稻(Oryza Sativa L. japonica nipponbare)的真实数据集进行了干旱胁迫。结果表明,陷阱能够比几种现有方法更准确地检测途径。陷阱有关http://biohealth.snu.ac.kr/software/trap/。

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