Next-generation sequencing of vertebrate experimental organisms

被引:31
|
作者
Turner, Daniel J. [1 ]
Keane, Thomas M. [1 ]
Sudbery, Ian [1 ]
Adams, David J. [1 ]
机构
[1] Wellcome Trust Sanger Inst, Cambridge CB10 1HH, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
SINGLE DNA-MOLECULES; GENETIC-ANALYSIS; GENOME SEQUENCE; RNA-SEQ; MOUSE;
D O I
10.1007/s00335-009-9187-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Next-generation sequencing technologies are revolutionizing biology by allowing for genome-wide transcription factor binding-site profiling, transcriptome sequencing, and more recently, whole-genome resequencing. While it is currently not possible to generate complete de novo assemblies of higher-vertebrate genomes using next-generation sequencing, improvements in sequence read lengths and throughput, coupled with new assembly algorithms for large data sets, will soon make this a reality. These developments will in turn spawn a revolution in how genomic data are used to understand genetics and how model organisms are used for disease gene discovery. This review provides an overview of the current next-generation sequencing platforms and the newest computational tools for the analysis of next-generation sequencing data. We also describe how next-generation sequencing may be applied in the context of vertebrate model organism genetics.
引用
收藏
页码:327 / 338
页数:12
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