CAMDA 2014: RNA-Seq数据的意义:从低级处理到功能分析

O. Moskvin, S. McIlwain, I. Ong
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引用次数: 5

摘要

许多RNA-Seq数据分析方法已经被开发出来,还有更多的方法正在积极开发中。在本文中,我们的重点是评估每个加工阶段的影响;从测序reads的预处理到比对/计数到计数归一化到差异表达测试到下游功能分析,基于推断的生物反应的功能模式。我们评估了6,912种技术和生物因素组合对转录组功能反应的影响。鉴于缺乏基本事实,我们使用了2个互补的评估标准:a)在2个类似比较中确定的功能模式的一致性,即自然毒性培养基和人工重组毒性培养基的效果,以及b)同一研究的RNA-Seq和微阵列版本结果的一致性。我们的研究结果表明,尽管在低级加工阶段(读取预处理、对齐和计数)和差异表达调用阶段具有很高的变异性,但它们对推断的生物反应模式的影响却非常低;相反,它们被功能富集方法的选择所掩盖。后者的影响程度与生物因素本身的影响相当。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
CAMDA 2014: Making sense of RNA-Seq data: From low-level processing to functional analysis
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 per se.
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