bioRxivMicrobiology
Comparison of Illumina MiSeq and the Ion Torrent PGM and S5 platforms for whole-genome sequencing of picornaviruses and caliciviruses
R. L. Marine, L. C. Magana, C. J. Castro, K. Zhao, A. Montmayeur, A. Schmidt, M. Diez-Valcarce, T. F. F. Ng, J. Vinje, C. C. Burns, W. A. Nix, P. A. Rota, M. S. Oberste
Abstract
Next-generation sequencing is a powerful tool for virological surveillance. While Illumina(R) and Ion Torrent(R) sequencing platforms are used extensively for generating viral RNA genome sequences, there is limited data comparing different platforms. We evaluated the Illumina MiSeq, Ion Torrent PGM and Ion Torrent S5 platforms using a panel of sixteen specimens containing picornaviruses and human caliciviruses (noroviruses and sapoviruses). The specimens were processed, using combinations of three library preparation and five sequencing kits, to assess the quality and completeness of assembled viral genomes, and an estimation of cost per sample to generate the data was calculated. The choice of library preparation kit and sequencing platform was found to impact the breadth of genome coverage and accuracy of consensus viral genomes. The Ion Torrent S5 outperformed the older Ion Torrent PGM platform in data quality and cost, and generated the highest proportion of reads for enterovirus D68 samples. However, indels at homopolymer regions impacted the accuracy of consensus genome sequences. For lower throughput sequencing runs (i.e., Ion Torrent 510 or Illumina MiSeq Nano V2), the cost per sample was lower on the MiSeq platform, whereas with higher throughput runs (Ion Torrent 530 or Illumina MiSeq V2) the cost per sample was comparable. These findings suggest that the Ion Torrent S5 and Illumina MiSeq platforms are both viable options for genomic sequencing of RNA viruses, each with specific advantages and tradeoffs.
- organism: virus
- assay: whole-genome sequencing
- research focus: benchmarking
- research focus: variant calling
- research focus: genome assembly
- research focus: differential expression
- approach: experimental assay
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Utility Analyses of AVITI Sequencing Chemistry
Silvia Liu, Caroline A. Obert, … Jianhua Luo·bioRxiv·Apr 18, 2024
- Rapid genotyping of viral samples using Illumina short-read sequencing data
Alex Váradi, Eszter Kaszab, … Levente Laczkó·bioRxiv·Mar 21, 2022
- Genomic Analysis of Human Noroviruses Using Hybrid Illumina-Nanopore Data
A. Flint, S. Reaume, … N. Nasheri·bioRxiv·Mar 30, 2021
- Analytical validity of nanopore sequencing for rapid SARS-CoV-2 genome analysis
Rowena Anne Bull, Thiruni N. Adikari, … Ira W. Deveson·Nature CommunicationsPeer-reviewed·Dec 9, 2020
- Rapid cost-effective viral genome sequencing by V-seq
Longhua Guo, James Boocock, … Yi A. Yin·bioRxiv·Aug 15, 2020
- Nanopore and Illumina Sequencing Reveal Different Viral Populations from Human Gut Samples
Ryan Cook, Andrea Telatin, … Evelien M. Adriaenssens·Microbial GenomicsPeer-reviewed·Apr 29, 2024