2019
DOI: 10.4310/cis.2019.v19.n1.a4
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Whole genome single nucleotide polymorphism genotyping of <i>Staphylococcus aureus</i>

Abstract: Next-generation sequencing technology enables routine detection of bacterial pathogens for clinical diagnostics and genetic research. Whole genome sequencing has been of importance in the epidemiologic analysis of bacterial pathogens. However, few whole genome sequencing-based genotyping pipelines are available for practical applications. Here, we present the whole genome sequencing-based single nucleotide polymorphism (SNP) genotyping method and apply to the evolutionary analysis of methicillin-resistant Stap… Show more

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Cited by 2 publications
(3 citation statements)
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“…However, in an emergency time, the complete genomes may not be available for SNP genotyping. In this case, the SNP variant calling process may directly use the raw NGS reads (Yin and Yau, 2019). The SNP variants then can be obtained by mapping the NGS reads to the reference genome by BWA alignments (Li, 2013), followed by GATK variant calling (McKenna et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
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“…However, in an emergency time, the complete genomes may not be available for SNP genotyping. In this case, the SNP variant calling process may directly use the raw NGS reads (Yin and Yau, 2019). The SNP variants then can be obtained by mapping the NGS reads to the reference genome by BWA alignments (Li, 2013), followed by GATK variant calling (McKenna et al, 2010).…”
Section: Discussionmentioning
confidence: 99%
“…Therefore, the genetic distance of two genomes corresponds to the Jaccard distance of their SNP variants. The Jaccard distance of SNP variants was adopted in the phylogenetic analysis of human or bacterial genomes (Comas et al, 2009;Yu et al, 2017;Yin and Yau, 2019). In this study, we use the Jaccard distance of the SNP mutations of virus genomes to measure the dissimilarity of virus isolates.…”
Section: Jaccard Distance Of the Snp Variantsmentioning
confidence: 99%
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