Dyer Nigel P, Shahrezaei Vahid, Hebenstreit Daniel
School of Life Sciences, University of Warwick, Coventry, UK.
Department of Mathematics, Imperial College London, London, UK.
PeerJ. 2019 Feb 4;7:e6222. doi: 10.7717/peerj.6222. eCollection 2019.
Protocols for preparing RNA sequencing (RNA-seq) libraries, most prominently "Smart-seq" variations, introduce global biases that can have a significant impact on the quantification of gene expression levels. This global bias can lead to drastic over- or under-representation of RNA in non-linear length-dependent fashion due to enzymatic reactions during cDNA production. It is currently not corrected by any RNA-seq software, which mostly focus on local bias in coverage along RNAs. This paper describes LiBiNorm, a simple command line program that mimics the popular htseq-count software and allows diagnostics, quantification, and global bias removal. LiBiNorm outputs gene expression data that has been normalized to correct for global bias introduced by the Smart-seq2 protocol. In addition, it produces data and several plots that allow insights into the experimental history underlying library preparation. The LiBiNorm package includes an R script that allows visualization of the main results. LiBiNorm is the first software application to correct for the global bias that is introduced by the Smart-seq2 protocol. It is freely downloadable at http://www2.warwick.ac.uk/fac/sci/lifesci/research/libinorm.
用于制备RNA测序(RNA-seq)文库的方案,最主要的是“Smart-seq”变体,会引入全局偏差,这可能对基因表达水平的定量产生重大影响。由于cDNA生成过程中的酶促反应,这种全局偏差可能导致RNA以非线性长度依赖的方式大幅过度或不足代表。目前没有任何RNA-seq软件对其进行校正,这些软件大多关注沿RNA覆盖的局部偏差。本文介绍了LiBiNorm,这是一个简单的命令行程序,它模仿了流行的htseq-count软件,并允许进行诊断、定量和全局偏差消除。LiBiNorm输出已标准化的基因表达数据,以校正Smart-seq2方案引入的全局偏差。此外,它还生成数据和几个图表,以便深入了解文库制备背后的实验过程。LiBiNorm软件包包括一个R脚本,用于可视化主要结果。LiBiNorm是第一个校正Smart-seq2方案引入的全局偏差的软件应用程序。可从http://www2.warwick.ac.uk/fac/sci/lifesci/research/libinorm免费下载。