Performance comparison of benchtop high-throughput sequencing platforms (original) (raw)
- Analysis
- Published: 22 April 2012
- Raju V Misra2,
- Timothy J Dallman2,
- Chrystala Constantinidou1,
- Saheer E Gharbia2,
- John Wain2,3 &
- …
- Mark J Pallen1
Nature Biotechnology volume 30, pages 434–439 (2012)Cite this article
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A Corrigendum to this article was published on 07 June 2012
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Abstract
Three benchtop high-throughput sequencing instruments are now available. The 454 GS Junior (Roche), MiSeq (Illumina) and Ion Torrent PGM (Life Technologies) are laser-printer sized and offer modest set-up and running costs. Each instrument can generate data required for a draft bacterial genome sequence in days, making them attractive for identifying and characterizing pathogens in the clinical setting. We compared the performance of these instruments by sequencing an isolate of Escherichia coli O104:H4, which caused an outbreak of food poisoning in Germany in 2011. The MiSeq had the highest throughput per run (1.6 Gb/run, 60 Mb/h) and lowest error rates. The 454 GS Junior generated the longest reads (up to 600 bases) and most contiguous assemblies but had the lowest throughput (70 Mb/run, 9 Mb/h). Run in 100-bp mode, the Ion Torrent PGM had the highest throughput (80–100 Mb/h). Unlike the MiSeq, the Ion Torrent PGM and 454 GS Junior both produced homopolymer-associated indel errors (1.5 and 0.38 errors per 100 bases, respectively).
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23 April 2012
On page 2, “error rates” has been corrected to “quality scores” in the sentence “Alignment quality scores measured in this way generally had good agreement with predicted scores, with the Ion Torrent PGM generally underestimating error rates and the other instruments slightly overestimating them (Supplementary Fig. 2).” The corrected sentence reads “Alignment quality scores measured in this way generally had good agreement with predicted scores, with the Ion Torrent PGM generally underestimating quality scores and the other instruments slightly overestimating them (Supplementary Fig. 2).”
07 June 2012
In the version of this article initially published online, in the Online Methods “Ion Torrent Sequencing” section, the sentence beginning with “Ten milligrams of this DNA was fragmented with a Bioruptor instrument….” should have read “Ten micrograms….” and in the “454 GS Junior sequencing” section, “(500 total)” should have read “(500 ng total).” The errors have been corrected in the PDF and HTML versions of this article.
References
- Pallen, M.J., Nelson, K. & Preston, G.M. Bacterial Pathogenomics (ASM Press, 2007).
- Metzker, M. Sequencing technologies—the next generation. Nat. Rev. Genet. 11, 31–46 (2010).
Article CAS Google Scholar - Glenn, T. Field guide to next-generation DNA sequencers. Mol. Ecol. Resour. 11, 759–769 (2011).
Article CAS Google Scholar - Pallen, M., Loman, N. & Penn, C. High-throughput sequencing and clinical microbiology: progress, opportunities and challenges. Curr. Opin. Microbiol. 13, 625–631 (2010).
Article CAS Google Scholar - Rothberg, J. et al. An integrated semiconductor device enabling non-optical genome sequencing. Nature 475, 348–352 (2011).
Article CAS Google Scholar - Bentley, D. et al. Accurate whole human genome sequencing using reversible terminator chemistry. Nature 456, 53–59 (2008).
Article CAS Google Scholar - Frank, C. et al. Epidemic profile of Shiga-toxin-producing Escherichia coli O104:H4 outbreak in Germany. N. Engl. J. Med. 365, 1771–1780 (2011).
Article CAS Google Scholar - Brzuszkiewicz, E. et al. Genome sequence analyses of two isolates from the recent Escherichia coli outbreak in Germany reveal the emergence of a new pathotype: entero-aggregative-haemorrhagic Escherichia coli (EAHEC). Arch. Microbiol. 193, 883–891 (2011).
Article CAS Google Scholar - Mellmann, A. et al. Prospective genomic characterization of the German enterohemorrhagic Escherichia coli O104:H4 outbreak by rapid next generation sequencing technology. PLoS ONE 6, e22751 (2011).
Article CAS Google Scholar - Rohde, H. et al. Open-source genomic analysis of Shiga-toxin-producing E. coli O104:H4. N. Engl. J. Med. 365, 718–724 (2011).
Article CAS Google Scholar - Rasko, D. et al. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N. Engl. J. Med. 365, 709–717 (2011).
Article CAS Google Scholar - Grad, Y. et al. Genomic epidemiology of the Escherichia coli O104:H4 outbreaks in Europe, 2011. Proc. Natl. Acad. Sci. USA 109, 3065–3070 (2012).
Article CAS Google Scholar - Ewing, B. & Green, P. Base-calling of automated sequencer traces using phred. II. Error probabilities. Genome Res. 8, 186–194 (1998).
Article CAS Google Scholar - Li, H. et al. The Sequence Alignment/Map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Article Google Scholar - Kingsford, C., Schatz, M. & Pop, M. Assembly complexity of prokaryotic genomes using short reads. BMC Bioinformatics 11, 21 (2010).
Article Google Scholar - Buffalo, V. qrqc: Quick Read Quality Control R package version 1.9.1 <http://bioinformatics.ucdavis.edu/> (2012).
- Chattaway, M., Dallman, T., Okeke, I. & Wain, J. Enteroaggregative E. coli O104 from an outbreak of HUS in Germany 2011, could it happen again? J. Infect. Dev. Ctries. 5, 425–436 (2011).
Article Google Scholar - Chaudhuri, R. et al. xBASE2: a comprehensive resource for comparative bacterial genomics. Nucleic Acids Res. 36, D543–546 (2008).
Article CAS Google Scholar - Delcher, A., Bratke, K., Powers, E. & Salzberg, S. Identifying bacterial genes and endosymbiont DNA with Glimmer. Bioinformatics 23, 673–679 (2007).
Article CAS Google Scholar - Lowe, T. & Eddy, S. tRNAscan-SE: a program for improved detection of transfer RNA genes in genomic sequence. Nucleic Acids Res. 25, 955–964 (1997).
Article CAS Google Scholar - Lagesen, K. et al. RNAmmer: consistent and rapid annotation of ribosomal RNA genes. Nucleic Acids Res. 35, 3100–3108 (2007).
Article CAS Google Scholar - Darling, A., Tritt, A., Eisen, J. & Facciotti, M. Mauve assembly metrics. Bioinformatics 27, 2756–2757 (2011).
Article CAS Google Scholar - Milne, I. et al. Tablet–next generation sequence assembly visualization. Bioinformatics 26, 401–402 (2010).
Article CAS Google Scholar - Li, H. & Durbin, R. Fast and accurate long-read alignment with Burrows-Wheeler transform. Bioinformatics 26, 589–595 (2010).
Article Google Scholar - Touchon, M. et al. Organised genome dynamics in the Escherichia coli species results in highly diverse adaptive paths. PLoS Genet. 5, e1000344 (2009).
Article Google Scholar
Acknowledgements
We gratefully acknowledge the blogging community for helpful discussion in the comments section of our blog (http://pathogenomics.bham.ac.uk/blog/), and in particular to B. Chevreux, J. Johnson, K. Robison and L. Nederbragt. We are grateful to C. Hercus at Novocraft for help with the Novoalign software and to A. Darling for help with Mauve Assembly Metrics. We thank Roche Diagnostics, UK, for 454 GS FLX+ and 454 FLX paired-end sequencing, technical support and helpful discussion. We thank Life Technologies for early access to 316 chips and instrument fluidics upgrade. We thank G. Smith and Illumina UK for early access to the MiSeq platform and public release of E. coli outbreak-strain data. We thank the three anonymous reviewers for their many helpful suggestions for improving the manuscript. The xBASE facility and N.J.L. are funded by BBSRC grant BBE0111791.
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Authors and Affiliations
- Centre for Systems Biology, University of Birmingham, Birmingham, UK
Nicholas J Loman, Chrystala Constantinidou & Mark J Pallen - Health Protection Agency, London, UK
Raju V Misra, Timothy J Dallman, Saheer E Gharbia & John Wain - School of Medicine, University of East Anglia, Norwich, UK
John Wain
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Contributions
N.J.L., J.W., S.E.G. and M.J.P. conceived the experiments; J.W. and S.G. supplied the strains; N.J.L., R.V.M. and T.J.D. carried out the bioinformatics analysis; C.C. performed the Ion Torrent sequencing; and S.E.G. and R.V.M. performed the 454 GS Junior sequencing. N.J.L. and M.J.P. wrote the manuscript. All authors commented on the manuscript.
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Correspondence toJohn Wain or Mark J Pallen.
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Competing interests
Mark J. Pallen was a winner of an Ion Torrent Personal Genome Machine in the European PGM grant program. Nicholas J. Loman has had expenses paid to speak at an Ion Torrent meeting organized by Life Technologies, and has received honoraria and expenses to speak at Illumina meetings. The other authors declare no financial interest.
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Loman, N., Misra, R., Dallman, T. et al. Performance comparison of benchtop high-throughput sequencing platforms.Nat Biotechnol 30, 434–439 (2012). https://doi.org/10.1038/nbt.2198
- Received: 19 December 2011
- Accepted: 30 March 2012
- Published: 22 April 2012
- Issue Date: May 2012
- DOI: https://doi.org/10.1038/nbt.2198