Ruan Xiaoan, Ruan Yijun
Genome Institute of Singapore, Singapore, Singapore.
Methods Mol Biol. 2012;809:535-62. doi: 10.1007/978-1-61779-376-9_35.
RNA-PET is a paired end tag (PET) sequencing method for full-length mRNA transcripts analysis using the next generation sequencer platforms such as Illumina GA and SOLiD. Unlike RNA-Seq method that sequences randomly sheared shotgun RNA short fragments, RNA-PET captures and sequences the 5' and 3' end tags of full-length cDNA fragments of all expressed genes in a biological sample. When mapped to reference genome, RNA-PET sequences can demarcate the boundaries of transcription units genome-wide, in addition to its ability to quantify the transcription level of each expression genes. Furthermore, the unique feature of RNA-PET is to identify fusion transcripts. Therefore, RNA-PET has been regarded as the best PET for genome annotation (1). Here in this chapter, we describe the details of the RNA-PET protocol and discuss the critical issues.
RNA-PET是一种配对末端标签(PET)测序方法,用于使用Illumina GA和SOLiD等新一代测序平台对全长mRNA转录本进行分析。与对随机剪切的鸟枪法RNA短片段进行测序的RNA-Seq方法不同,RNA-PET捕获并测序生物样品中所有表达基因的全长cDNA片段的5'和3'末端标签。当映射到参考基因组时,RNA-PET序列除了能够量化每个表达基因的转录水平外,还能在全基因组范围内划定转录单元的边界。此外,RNA-PET的独特功能是识别融合转录本。因此,RNA-PET被认为是用于基因组注释的最佳PET(1)。在本章中,我们将描述RNA-PET方案的详细信息并讨论关键问题。