Han Leng, Vickers Kasey C, Samuels David C, Guo Yan
Brief Bioinform. 2015 Jul;16(4):629-39. doi: 10.1093/bib/bbu032. Epub 2014 Sep 22.
Recent advances in RNA library preparation methods, platform accessibility and cost efficiency have allowed high-throughput RNA sequencing (RNAseq) to replace conventional hybridization microarray platforms as the method of choice for mRNA profiling and transcriptome analyses. RNAseq is a powerful technique to profile both long and short RNA expression, and the depth of information gained from distinct RNAseq methods is striking and facilitates discovery. In addition to expression analysis, distinct RNAseq approaches also allow investigators the ability to assess transcriptional elongation, DNA variance and exogenous RNA content. Here we review the current state of the art in transcriptome sequencing and address epigenetic regulation, quantification of transcription activation, RNAseq output and a diverse set of applications for RNAseq data. We detail how RNAseq can be used to identify allele-specific expression, single-nucleotide polymorphisms and somatic mutations and discuss the benefits and limitations of using RNAseq to monitor DNA characteristics. Moreover, we highlight the power of combining RNA- and DNAseq methods for genomic analysis. In summary, RNAseq provides the opportunity to gain greater insight into transcriptional regulation and output than simply miRNA and mRNA profiling.
RNA文库制备方法、平台可及性和成本效益方面的最新进展,已使高通量RNA测序(RNAseq)取代传统杂交微阵列平台,成为mRNA谱分析和转录组分析的首选方法。RNAseq是一种强大的技术,可对长RNA和短RNA的表达进行谱分析,并且从不同RNAseq方法获得的信息深度惊人,有助于新发现。除表达分析外,不同的RNAseq方法还使研究人员能够评估转录延伸、DNA变异和外源RNA含量。在此,我们综述转录组测序的当前技术水平,并探讨表观遗传调控、转录激活定量、RNAseq输出以及RNAseq数据的一系列不同应用。我们详细介绍了如何使用RNAseq来鉴定等位基因特异性表达、单核苷酸多态性和体细胞突变,并讨论了使用RNAseq监测DNA特征的优点和局限性。此外,我们强调了将RNA测序和DNA测序方法相结合用于基因组分析的强大功能。总之,与单纯的miRNA和mRNA谱分析相比,RNAseq提供了一个更深入了解转录调控和输出的机会。