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Making sense of RNA-Seq data: From low-level processing to functional analysis

机译:理解RNA-Seq数据:从低级处理到功能分析

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Numerous methods of RNA-Seq data analysis have been developed, and there are more under active development. In this paper, our focus is on evaluating the impact of each processing stage; from pre-processing of sequencing reads to alignment/counting to count normalization to differential expression testing to downstream functional analysis, on the inferred functional pattern of biological response. We assess the impact of 6,912 combinations of technical and biological factors on the resulting signature of transcriptomic functional response. Given the absence of the ground truth, we use 2 complementary evaluation criteria: a) consistency of the functional patterns identified in 2 similar comparisons, namely effects of a naturally-toxic medium and a medium with artificially reconstituted toxicity, and b) consistency of the results in RNA-Seq and microarray versions of the same study. Our results show that despite high variability at the low-level processing stage (read pre-processing, alignment and counting) and the differential expression calling stage, their impact on the inferred pattern of biological response was surprisingly low; they were instead overshadowed by the choice of the functional enrichment method. The latter have an impact comparable in magnitude to the impact of biological factors perse.
机译:已经开发了许多RNA-Seq数据分析的方法,并且正在积极开发中。在本文中,我们的重点是评估每个处理阶段的影响。从推断的生物学反应功能模式,从测序读物的预处理到比对/计数以计数归一化到差异表达测试再到下游功能分析。我们评估了6,912种技术和生物学因素组合对转录组功能反应的最终特征的影响。鉴于缺乏基本事实,我们使用2个补充评估标准:a)在2个相似的比较中确定的功能模式的一致性,即天然毒性介质和具有人工重构毒性的介质的影响,以及b)一致性。得出同一研究的RNA-Seq和微阵列版本。我们的结果表明,尽管在低级处理阶段(读取预处理,比对和计数)和差异表达调用阶段存在很大的可变性,但它们对推断的生物反应模式的影响却非常低。相反,它们被功能丰富方法的选择所笼罩。后者的影响在大小上可与生物因素本身的影响相媲美。

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