Bayega Anthony, Wang Yu Chang, Oikonomopoulos Spyros, Djambazian Haig, Fahiminiya Somayyeh, Ragoussis Jiannis
Department of Human Genetics, McGill University and Genome Quebec Innovation Centre, McGill University, Montréal, QC, Canada.
Cancer Research Program, The Research Institute of the McGill University Health Centre, Montreal, QC, Canada.
Methods Mol Biol. 2018;1783:121-147. doi: 10.1007/978-1-4939-7834-2_6.
RNA sequencing using next-generation sequencing (NGS, RNA-Seq) technologies is currently the standard approach for gene expression profiling, particularly for large-scale high-throughput studies. NGS technologies comprise short-read RNA-Seq (dominated by Illumina) and long-read RNA-Seq technologies provided by Pacific Bioscience (PacBio) and Oxford Nanopore Technologies (ONT). Although short-read sequencing technologies are the most widely used, long-read technologies are increasingly becoming the standard approach for de novo transcriptome assembly and isoform expression quantification due to the complex nature of the transcriptome which consists of variable lengths of transcripts and multiple alternatively spliced isoforms for most genes. In this chapter, we describe experimental procedures for library preparation, sequencing, and associated data analysis approaches for PacBio and ONT with a major focus on full length cDNA synthesis, de novo transcriptome assembly, and isoform quantification.
使用下一代测序(NGS,RNA测序)技术进行RNA测序是目前基因表达谱分析的标准方法,特别是对于大规模高通量研究。NGS技术包括短读长RNA测序(以Illumina为主)以及太平洋生物科学公司(PacBio)和牛津纳米孔技术公司(ONT)提供的长读长RNA测序技术。尽管短读长测序技术使用最为广泛,但由于转录组的复杂性质(大多数基因由可变长度的转录本和多个可变剪接异构体组成),长读长技术正日益成为从头转录组组装和异构体表达定量的标准方法。在本章中,我们描述了PacBio和ONT文库制备、测序及相关数据分析方法的实验步骤,主要侧重于全长cDNA合成、从头转录组组装和异构体定量。