RNA-Seq methods for transcriptome analysis

被引:434
|
作者
Hrdlickova, Radmila [1 ]
Toloue, Masoud [1 ]
Tian, Bin [2 ]
机构
[1] Bioo Sci Inc, Austin, TX 78744 USA
[2] Rutgers New Jersey Med Sch, Dept Microbiol Biochem & Mol Genet, Newark, NJ 07103 USA
关键词
LIBRARY PREPARATION PROTOCOL; GENE-EXPRESSION; MESSENGER-RNA; ALTERNATIVE CLEAVAGE; NONCODING RNAS; IN-VIVO; SEQUENCING METHOD; CELL-RECEPTOR; CDNA LIBRARY; HUMAN BRAIN;
D O I
10.1002/wrna.1364
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Deep sequencing has been revolutionizing biology and medicine in recent years, providing single base-level precision for our understanding of nucleic acid sequences in high throughput fashion. Sequencing of RNA, or RNA-Seq, is now a common method to analyze gene expression and to uncover novel RNA species. Aspects of RNA biogenesis and metabolism can be interrogated with specialized methods for cDNA library preparation. In this study, we review current RNA-Seq methods for general analysis of gene expression and several specific applications, including isoform and gene fusion detection, digital gene expression profiling, targeted sequencing and single-cell analysis. In addition, we discuss approaches to examine aspects of RNA in the cell, technical challenges of existing RNA-Seq methods, and future directions. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页数:17
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