Assessing Illumina technology for the high-throughput sequencing of bacteriophage genomes

被引:27
|
作者
Rihtman, Branko [1 ]
Meaden, Sean [2 ]
Clokie, Martha R. J. [3 ]
Koskella, Britt [2 ,4 ]
Millard, Andrew D. [5 ]
机构
[1] Univ Warwick, Sch Life Sci, Coventry CV4 7AL, W Midlands, England
[2] Univ Exeter, Coll Life & Environm Sci, Exeter EX4 4QJ, Devon, England
[3] Univ Leicester, Dept Infect Immun & Inflammat, Leicester LE1 7RH, Leics, England
[4] Univ Calif Berkeley, Dept Integrat Biol, Berkeley, CA 94720 USA
[5] Univ Warwick, Warwick Med Sch, Coventry CV4 7AL, W Midlands, England
来源
PEERJ | 2016年 / 4卷
关键词
Bacteriophage; Genome; Assembly; Sequencing; Illumina; MARINE SYNECHOCOCCUS STRAINS; COMPLETE NUCLEOTIDE-SEQUENCE; VIRAL METAGENOMICS; PHOTOSYNTHESIS GENES; INFLUENZAE RD; DNA; VIRUSES; GENERATION; RESISTANCE; DIVERSITY;
D O I
10.7717/peerj.2055
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bacteriophages are the most abundant biological entities on the planet, playing crucial roles in the shaping of bacterial populations. Phages have smaller genomes than their bacterial hosts, yet there are currently fewer fully sequenced phage than bacterial genomes. We assessed the suitability of Illumina technology for high-throughput sequencing and subsequent assembly of phage genomes. In silico datasets reveal that 30x coverage is sufficient to correctly assemble the complete genome of similar to 98.5% of known phages, with experimental data confirming that the majority of phage genomes can be assembled at 30x coverage. Furthermore, in silico data demonstrate it is possible to co-sequence multiple phages from different hosts, without introducing assembly errors.
引用
收藏
页数:21
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