2010
DOI: 10.1186/1471-2105-11-461
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Pan-genome sequence analysis using Panseq: an online tool for the rapid analysis of core and accessory genomic regions

Abstract: BackgroundThe pan-genome of a bacterial species consists of a core and an accessory gene pool. The accessory genome is thought to be an important source of genetic variability in bacterial populations and is gained through lateral gene transfer, allowing subpopulations of bacteria to better adapt to specific niches. Low-cost and high-throughput sequencing platforms have created an exponential increase in genome sequence data and an opportunity to study the pan-genomes of many bacterial species. In this study, … Show more

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Cited by 248 publications
(233 citation statements)
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“…Unique sequences were identified based on alignments of homologous sequences performed using SeqMan software (Lasergene 8; DNASTAR Inc.). Somatic probes were designed based on publicly available sequences and on sequences determined inhouse for gene targets (Table 2) (32). Similarly, a unique rhs-like gene sequence (SG1045) of Salmonella Gallinarum (NC_011274) was used to design a serovar-specific probe.…”
Section: Resultsmentioning
confidence: 99%
“…Unique sequences were identified based on alignments of homologous sequences performed using SeqMan software (Lasergene 8; DNASTAR Inc.). Somatic probes were designed based on publicly available sequences and on sequences determined inhouse for gene targets (Table 2) (32). Similarly, a unique rhs-like gene sequence (SG1045) of Salmonella Gallinarum (NC_011274) was used to design a serovar-specific probe.…”
Section: Resultsmentioning
confidence: 99%
“…Core and accessory genomes were estimated using whole genes and 250 base windows, identified using PANSEQ (55), as the unit of comparison. These approaches gave similar results, and PANSEQ results are used here (Fig.…”
Section: Methodsmentioning
confidence: 99%
“…The genomes are classified according to geographic location (Atlantic vs Pacific) and environment type (oil reservoir vs marine vent). For networks (a) and (b), the data were obtained using PanSeq (Laing et al, 2010). Core SNPs were required to be present in all 7 genomes, whereas the genomic fragments were considered shared if they were at least 80% identical.…”
Section: Resultsmentioning
confidence: 99%
“…Pan-genome calculations were performed in Panseq (Laing et al, 2010) using a fragment size of 500 bp and 80% identity cutoff for the analyses of TM-group genomes, and 90% identity cutoff for the analyses of TM-group and genomes assembled from metagenomes (to confidently exclude possible contamination). The data matrices of shared core SNPs and shared 500 bp fragments were converted into uncorrected distances and visualized in SplitsTree 4 (Huson and Bryant, 2006) using NeighborNet clustering.…”
Section: Gene Content and Genome Alignmentsmentioning
confidence: 99%