Hoeijmakers Wieteke A M, Bártfai Richárd, Stunnenberg Hendrik G
Department of Molecular Biology, Nijmegen Center for Molecular Life Sciences, Nijmegen, The Netherlands.
Methods Mol Biol. 2013;923:221-39. doi: 10.1007/978-1-62703-026-7_15.
Transcriptome analysis by next-generation sequencing (RNA-seq) allows investigation of a transcriptome at unsurpassed resolution. One major benefit is that RNA-seq is independent of a priori knowledge on the sequence under investigation, thereby also allowing analysis of poorly characterized Plasmodium species. Here we provide a detailed protocol for RNA isolation and fragmentation, ribosomal RNA depletion, and cDNA synthesis that enables the preparation of a sequencing library from 1 to 2 μg of total RNA. Although we focus our discussion on the quantitative measurement of gene expression, this protocol is suited for many applications of RNA-seq and allows analysis of most RNA species.
通过新一代测序(RNA测序)进行转录组分析能够以无与伦比的分辨率研究转录组。一个主要优点是RNA测序不依赖于对所研究序列的先验知识,从而也能够分析特征描述较少的疟原虫物种。在这里,我们提供了一个详细的方案,用于RNA分离和片段化、核糖体RNA去除以及cDNA合成,该方案能够从1至2μg总RNA制备测序文库。尽管我们的讨论重点是基因表达的定量测量,但该方案适用于RNA测序的许多应用,并能够分析大多数RNA种类。