Evidence map›Paper›PMID 29890941›Full record

ArticleBMC bioinformatics2018

Variant site strain typer (VaST): efficient strain typing using a minimal number of variant genomic sites.

Tara N Furstenau, Jill H Cocking, Jason W Sahl, Viacheslav Y Fofanov

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Tara N FurstenauThe School of Informatics, Computing, and Cyber Systems, Northern Arizona University, 1295 S Knoles Dr., Flagstaff, Arizona, 86001, USA.
Jill H CockingThe School of Informatics, Computing, and Cyber Systems, Northern Arizona University, 1295 S Knoles Dr., Flagstaff, Arizona, 86001, USA.
Jason W SahlPathogen and Microbiome Institute, Northern Arizona University, 1395 S Knoles Dr., Flagstaff, Arizona, 86001, USA.
Viacheslav Y FofanovThe School of Informatics, Computing, and Cyber Systems, Northern Arizona University, 1295 S Knoles Dr., Flagstaff, Arizona, 86001, USA. Viacheslav.Fofanov@nau.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTargeted PCR amplicon sequencing (TAS) techniques provide a sensitive, scalable, and cost-effective way to query and identify closely related bacterial species and strains. Typically, this is accomplished by targeting housekeeping genes that provide resolution down to the family, genera, and sometimes species level. Unfortunately, this level of resolution is not sufficient in many applications where strain-level identification of bacteria is required (biodefense, forensics, clinical diagnostics, and outbreak investigations). Adding more genomic targets will increase the resolution, but the challenge is identifying the appropriate targets. VaST was developed to address this challenge by finding the minimum number of targets that, in combination, achieve maximum strain-level resolution for any strain complex. The final combination of target regions identified by the algorithm produce a unique haplotype for each strain which can be used as a fingerprint for identifying unknown samples in a TAS assay. VaST ensures that the targets have conserved primer regions so that the targets can be amplified in all of the known strains and it also favors the inclusion of targets with basal variants which makes the set more robust when identifying previously unseen strains.

resultsWe analyzed VaST's performance using a number of different pathogenic species that are relevant to human disease outbreaks and biodefense. The number of targets required to achieve full resolution ranged from 20 to 88% fewer sites than what would be required in the worst case and most of the resolution is achieved within the first 20 targets. We computationally and experimentally validated one of the VaST panels and found that the targets led to accurate phylogenetic placement of strains, even when the strains were not a part of the original panel design.

conclusionsVaST is an open source software that, when provided a set of variant sites, can find the minimum number of sites that will provide maximum resolution of a strain complex, and it has many different run-time options that can accommodate a wide range of applications. VaST can be an effective tool in the design of strain identification panels that, when combined with TAS technologies, offer an efficient and inexpensive strain typing protocol.

Indexed as

Genes, BacterialGenome, BacterialPolymorphism, Single NucleotideBacteriaBacterial Typing TechniquesGenomicsGenotypeHumansMultilocus Sequence TypingPhylogenyBacterial strain typingSingle nucleotide polymorphismsTargeted PCR Amplicon sequencing

Identifiers

PMID29890941
PMCPMC5996513

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.