2019
DOI: 10.1016/j.fm.2019.103270
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Genetic diversity, virulence factors and farm-to-table spread pattern of Vibrio parahaemolyticus food-associated isolates

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Cited by 39 publications
(45 citation statements)
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“…The number of contigs and average size of assemblies were 163 (46-495, > 500 bp) and 4.0 Mb (3.9-4.3), with an average of 81-fold (54-96) depth for each V. cholerae genome. SNPs were identified as previously described [32,33]. Firstly, the assemblies were aligned against the reference genome using MUMmer v3.1 [34], to generate the whole genome alignment and identify SNPs in the core genome (regions present in all isolates).…”
Section: Genome Sequencing and Variant Callingmentioning
confidence: 99%
“…The number of contigs and average size of assemblies were 163 (46-495, > 500 bp) and 4.0 Mb (3.9-4.3), with an average of 81-fold (54-96) depth for each V. cholerae genome. SNPs were identified as previously described [32,33]. Firstly, the assemblies were aligned against the reference genome using MUMmer v3.1 [34], to generate the whole genome alignment and identify SNPs in the core genome (regions present in all isolates).…”
Section: Genome Sequencing and Variant Callingmentioning
confidence: 99%
“…By calculating the pairwise SNP distances between all 233 isolates, we defined semiclonal groups (SCG), among which the sequence differences are fewer than 2,000 SNPs, as suggested by Yang et al (14). Thirty-two SCGs were identified, with each SCG including 2 to 19 isolates.…”
Section: Resultsmentioning
confidence: 99%
“…SNPs located in the recombination regions were removed by ClonalFrameML ( 30 ). Taking 2,000 as the threshold of pairwise SNP distance between strains ( 14 ), we defined semiclonal groups (SCGs) in our analyzed data set. Meanwhile, we recalculated the pairwise SNP distance between isolates of each SCG to identify clones which were defined as the genomes with fewer than 10 SNPs differences ( 14 ).…”
Section: Methodsmentioning
confidence: 99%
“…NC_003143.1) using MUMmer (v3.0) (Kurtz et al, 2004) to generate whole-genome alignments and to identify single nucleotide polymorphisms (SNPs) in the core genome. The raw sequencing reads were mapped to the assemblies to evaluate the SNP accuracy using SOAPaligner as described previously (Yang et al, 2019). This process excludes unreliable SNPs located in repeated regions with low-quality scores (<20) or supported by few reads (<10 paired-end reads).…”
Section: Phylogeny Reconstructionmentioning
confidence: 99%