A large genome center's improvements to the Illumina sequencing system

被引:514
作者
Quail, Michael A. [1 ]
Kozarewa, Iwanka [1 ]
Smith, Frances [1 ]
Scally, Aylwyn [1 ]
Stephens, Philip J. [1 ]
Durbin, Richard [1 ]
Swerdlow, Harold [1 ]
Turner, Daniel J. [1 ]
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
D O I
10.1038/nmeth.1270
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The Wellcome Trust Sanger Institute is one of the world's largest genome centers, and a substantial amount of our sequencing is performed with 'next-generation' massively parallel sequencing technologies: in June 2008 the quantity of purity-filtered sequence data generated by our Genome Analyzer (Illumina) platforms reached 1 terabase, and our average weekly Illumina production output is currently 64 gigabases. Here we describe a set of improvements we have made to the standard Illumina protocols to make the library preparation more reliable in a high-throughput environment, to reduce bias, tighten insert size distribution and reliably obtain high yields of data.
引用
收藏
页码:1005 / 1010
页数:6
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