Standards for sequencing viral genomes in the era of high-throughput sequencing
- PMID: 24939889
- PMCID: PMC4068259
- DOI: 10.1128/mBio.01360-14
Standards for sequencing viral genomes in the era of high-throughput sequencing
Abstract
Thanks to high-throughput sequencing technologies, genome sequencing has become a common component in nearly all aspects of viral research; thus, we are experiencing an explosion in both the number of available genome sequences and the number of institutions producing such data. However, there are currently no common standards used to convey the quality, and therefore utility, of these various genome sequences. Here, we propose five "standard" categories that encompass all stages of viral genome finishing, and we define them using simple criteria that are agnostic to the technology used for sequencing. We also provide genome finishing recommendations for various downstream applications, keeping in mind the cost-benefit trade-offs associated with different levels of finishing. Our goal is to define a common vocabulary that will allow comparison of genome quality across different research groups, sequencing platforms, and assembly techniques.
Copyright © 2014 Ladner et al.
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Comment in
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Expanding the conversation on high-throughput virome sequencing standards to include consideration of microbial contamination sources.mBio. 2014 Oct 28;5(6):e01989. doi: 10.1128/mBio.01989-14. mBio. 2014. PMID: 25352620 Free PMC article. No abstract available.
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Reply to "Expanding the conversation on high-throughput virome sequencing standards to include consideration of microbial contamination sources".mBio. 2014 Oct 28;5(6):e02084. doi: 10.1128/mBio.02084-14. mBio. 2014. PMID: 25352625 Free PMC article. No abstract available.
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