Targeted sequencing for gene discovery and quantification using RNA CaptureSeq

被引:119
作者
Mercer, Tim R. [1 ]
Clark, Michael B. [1 ,2 ]
Crawford, Joanna [2 ]
Brunck, Marion E. [3 ]
Gerhardt, Daniel J. [4 ]
Taft, Ryan J. [2 ]
Nielsen, Lars K. [3 ]
Dinger, Marcel E. [1 ]
Mattick, John S. [1 ]
机构
[1] Garvan Inst Med Res, Sydney, NSW, Australia
[2] Univ Queensland, Inst Mol Biosci, Brisbane, Qld, Australia
[3] Univ Queensland, Australian Inst Bioengn & Nanotechnol, Brisbane, Qld, Australia
[4] Univ Queensland, Mater Res Inst, Translat Res Inst, Woolloongabba, Qld, Australia
基金
英国医学研究理事会;
关键词
EXPRESSION ANALYSIS; MULTIPLEX AMPLIFICATION; ISOFORM DISCOVERY; LARGE SETS; SEQ DATA; VARIANTS; TRANSCRIPTOMES; IDENTIFICATION; LANDSCAPE; ALIGNMENT;
D O I
10.1038/nprot.2014.058
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
RNA sequencing (RNAseq) samples the majority of expressed genes infrequently, owing to the large size, complex splicing and wide dynamic range of eukaryotic transcriptomes. This results in sparse sequencing coverage that can hinder robust isoform assembly and quantification. RNARNARNA capture sequencing (CaptureSeq) addresses this challenge by using oligonucleotide probes to capture selected genes or regions of interest for targeted sequencing. Targeted RNARNARNAseq provides enhanced coverage for sensitive gene discovery, robust transcript assembly and accurate gene quantification. Here we describe a detailed protocol for all stages of RNARNARNA CaptureSeq, from initial probe design considerations and capture of targeted genes to final assembly and quantification of captured transcripts. Initial probe design and final analysis can take less than 1 d, whereas the central experimental capture stage requires similar to 7 d.
引用
收藏
页码:989 / 1009
页数:21
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