Arrigoni Alberto, Ranzani Valeria, Rossetti Grazisa, Panzeri Ilaria, Abrignani Sergio, Bonnal Raoul J P, Pagani Massimiliano
Istituto Nazionale Genetica Molecolare 'Romeo ed Enrica Invernizzi', Via F. Sforza 35, 20122, Milan, Italy.
Department of Clinical Sciences and Community Health, Università degli Studi di Milano, Via Festa del Perdono 7, 20122, Milan, Italy.
Methods Mol Biol. 2016;1480:125-35. doi: 10.1007/978-1-4939-6380-5_11.
RNA-Seq is an approach to transcriptome profiling that uses deep-sequencing technologies to detect and accurately quantify RNA molecules originating from a genome at a given moment in time. In recent years, the advent of RNA-Seq has facilitated genome-wide expression profiling, including the identification of novel and rare transcripts like noncoding RNAs and novel alternative splicing isoforms.Here, we describe the analytical steps required for the identification and characterization of noncoding RNAs starting from RNA-Seq raw samples, with a particular emphasis on long noncoding RNAs (lncRNAs).
RNA测序是一种转录组分析方法,它利用深度测序技术在特定时刻检测并准确量化源自基因组的RNA分子。近年来,RNA测序技术的出现推动了全基因组表达谱分析,包括鉴定新型和稀有转录本,如非编码RNA以及新型可变剪接异构体。在此,我们描述了从RNA测序原始样本开始鉴定和表征非编码RNA所需的分析步骤,尤其着重于长链非编码RNA(lncRNA)。