A single chromosome assembly of Bacteroides fragilis strain BE1 from Illumina and MinION nanopore sequencing data

被引:42
作者
Risse, Judith [1 ]
Thomson, Marian [1 ]
Patrick, Sheila [2 ]
Blakely, Garry [3 ]
Koutsovoulos, Georgios [4 ]
Blaxter, Mark [1 ,4 ]
Watson, Mick [1 ,5 ]
机构
[1] Univ Edinburgh, Sch Biol Sci, Edinburgh Genom, Edinburgh EH9 3FL, Midlothian, Scotland
[2] Queens Univ Belfast, Sch Med Dent & Biomed Sci, Ctr Infect & Immun, Belfast, Antrim, North Ireland
[3] Univ Edinburgh, Sch Biol Sci, Inst Cell Biol, Edinburgh EH9 3BF, Midlothian, Scotland
[4] Univ Edinburgh, Sch Biol Sci, Inst Evolutionary Biol, Edinburgh EH9 3FL, Midlothian, Scotland
[5] Univ Edinburgh, Roslin Inst, Easter Bush EH25 9RG, Midlothian, Scotland
基金
英国生物技术与生命科学研究理事会;
关键词
EXTENSIVE DNA INVERSIONS; GENOMES;
D O I
10.1186/s13742-015-0101-6
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Second and third generation sequencing technologies have revolutionised bacterial genomics. Short-read Illumina reads result in cheap but fragmented assemblies, whereas longer reads are more expensive but result in more complete genomes. The Oxford Nanopore MinION device is a revolutionary mobile sequencer that can produce thousands of long, single molecule reads. Results: We sequenced Bacteroides fragilis strain BE1 using both the Illumina MiSeq and Oxford Nanopore MinION platforms. We were able to assemble a single chromosome of 5.18 Mb, with no gaps, using publicly available software and commodity computing hardware. We identified gene rearrangements and the state of invertible promoters in the strain. Conclusions: The single chromosome assembly of Bacteroides fragilis strain BE1 was achieved using only modest amounts of data, publicly available software and commodity computing hardware. This combination of technologies offers the possibility of ultra-cheap, high quality, finished bacterial genomes.
引用
收藏
页数:7
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