RNA质量和数量的变化是微阵列表达数据批次效应的主要来源。

Mario Fasold, Hans Binder
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引用次数: 13

摘要

微阵列对基因组级表达分析的巨大效用受到批效应的广泛存在的挑战,批效应尤其在大数据集内偏倚表达测量。这些不需要的技术工件会模糊生物变异,从而显著降低分析结果的可靠性。哪些是导致批次效应的主要技术来源在很大程度上是未知的。我们在此定量评估几种已知技术对微阵列表达结果的影响。特别是,我们关注RNA降解,RNA数量和序列偏差等重要因素,包括多重鸟嘌呤效应。我们发现,RNA质量和RNA数量的共同变化不仅会导致低质量的表达结果,而且这两个因素还与样品的批效应和生物学特性有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Variation of RNA Quality and Quantity Are Major Sources of Batch Effects in Microarray Expression Data.

Variation of RNA Quality and Quantity Are Major Sources of Batch Effects in Microarray Expression Data.

Variation of RNA Quality and Quantity Are Major Sources of Batch Effects in Microarray Expression Data.

Variation of RNA Quality and Quantity Are Major Sources of Batch Effects in Microarray Expression Data.

The great utility of microarrays for genome-scale expression analysis is challenged by the widespread presence of batch effects, which bias expression measurements in particular within large data sets. These unwanted technical artifacts can obscure biological variation and thus significantly reduce the reliability of the analysis results. It is largely unknown which are the predominant technical sources leading to batch effects. We here quantitatively assess the prevalence and impact of several known technical effects on microarray expression results. Particularly, we focus on important factors such as RNA degradation, RNA quantity, and sequence biases including multiple guanine effects. We find that the common variation of RNA quality and RNA quantity can not only yield low-quality expression results, but that both factors also correlate with batch effects and biological characteristics of the samples.

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来源期刊
自引率
0.00%
发文量
0
审稿时长
11 weeks
期刊介绍: High-Throughput (formerly Microarrays, ISSN 2076-3905) is a multidisciplinary peer-reviewed scientific journal that provides an advanced forum for the publication of studies reporting high-dimensional approaches and developments in Life Sciences, Chemistry and related fields. Our aim is to encourage scientists to publish their experimental and theoretical results based on high-throughput techniques as well as computational and statistical tools for data analysis and interpretation. The full experimental or methodological details must be provided so that the results can be reproduced. There is no restriction on the length of the papers. High-Throughput invites submissions covering several topics, including, but not limited to: Microarrays, DNA Sequencing, RNA Sequencing, Protein Identification and Quantification, Cell-based Approaches, Omics Technologies, Imaging, Bioinformatics, Computational Biology/Chemistry, Statistics, Integrative Omics, Drug Discovery and Development, Microfluidics, Lab-on-a-chip, Data Mining, Databases, Multiplex Assays.
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