Robust high-throughput prokaryote de novo assembly and improvement pipeline for Illumina data

被引:180
作者
Page, Andrew J. [1 ]
De Silva, Nishadi [1 ]
Hunt, Martin [1 ]
Quail, Michael A. [2 ]
Parkhill, Julian [3 ]
Harris, Simon R. [3 ]
Otto, Thomas D. [4 ]
Keane, Jacqueline A. [1 ]
机构
[1] Wellcome Trust Sanger Inst, Pathogen Informat, Wellcome Genome Campus, Hinxton CB10 1SA, Cambs, England
[2] Wellcome Trust Sanger Inst, Biochem Dev, Wellcome Genome Campus, Hinxton CB10 1SA, Cambs, England
[3] Wellcome Trust Sanger Inst, Pathogen Genom, Wellcome Genome Campus, Hinxton CB10 1SA, Cambs, England
[4] Wellcome Trust Sanger Inst, Parasite Genom, Wellcome Genome Campus, Hinxton CB10 1SA, Cambs, England
基金
英国惠康基金;
关键词
illumina; assembly; high-throughput; prokaryotic; GENOME SEQUENCE; ALGORITHM; EVOLUTION;
D O I
10.1099/mgen.0.000083
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The rapidly reducing cost of bacterial genome sequencing has lead to its routine use in large-scale microbial analysis. Though mapping approaches can be used to find differences relative to the reference, many bacteria are subject to constant evolutionary pressures resulting in events such as the loss and gain of mobile genetic elements, horizontal gene transfer through recombination and genomic rearrangements. De novo assembly is the reconstruction of the underlying genome sequence, an essential step to understanding bacterial genome diversity. Here we present a high-throughput bacterial assembly and improvement pipeline that has been used to generate nearly 20 000 annotated draft genome assemblies in public databases. We demonstrate its performance on a public data set of 9404 genomes. We find all the genes used in multi-locus sequence typing schema present in 99.6 % of assembled genomes. When tested on low-,neutral-and high-GC organisms, more than 94 % of genes were present and completely intact. The pipeline has been proven to be scalable and robust with a wide variety of datasets without requiring human intervention. All of the software is available on GitHub under the GNU GPL open source license.
引用
收藏
页数:7
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