2018
DOI: 10.1093/bioinformatics/bty212
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SnapperDB: a database solution for routine sequencing analysis of bacterial isolates

Abstract: SnapperDB is implemented as a python application under the open source BSD license. All code and user guides are available at https://github.com/phe-bioinformatics/snapperdb. Reference genomes and SnapperDB configs are available at https://github.com/phe-bioinformatics/snapperdb_references.

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Cited by 173 publications
(190 citation statements)
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“…Salmonella genomes have been assembled and stored in Enterobase (https://enterobase.warwick.ac.uk/). The availability of thousands of whole-genome sequences of S. Typhimurium has given epidemiological investigators an unprecedented ability to discover outbreaks, which involve S. Typhimurium isolates that vary by fewer than five core-genome SNPs [5]. However, Enterobase only contained four genome sequences of Colombian S. Typhimurium.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Salmonella genomes have been assembled and stored in Enterobase (https://enterobase.warwick.ac.uk/). The availability of thousands of whole-genome sequences of S. Typhimurium has given epidemiological investigators an unprecedented ability to discover outbreaks, which involve S. Typhimurium isolates that vary by fewer than five core-genome SNPs [5]. However, Enterobase only contained four genome sequences of Colombian S. Typhimurium.…”
Section: Introductionmentioning
confidence: 99%
“…Since the 1990s, monophasic variants of S. Typhimurium, S. 4, [5],12:i:-(MVST) have arisen at high frequency across the world. MVST is a variant of S. Typhimurium that does not express the phase 2 H-antigen [6].…”
Section: Introductionmentioning
confidence: 99%
“…Upon the launch of the urgent inquiries from Scotland (18 January 2016) and the Netherlands (25 August 2016) in the Epidemic Intelligence Information System for Food-and Waterborne Diseases and Zoonoses (EPIS-FWD), an EU/EEA-level investigation into a multi-country outbreak of S. Enteritidis was initiated. For the EU outbreak case definition [1] whole genome sequencing (WGS)-based typing was used, applying the Public Health England's (PHE) single nucleotide polymorphism (SNP) calling pipeline PHEnix (https://github.com/phe-bioinformatics/PHEnix) and nomenclature implemented in PHE SnapperDB [2][3][4]. Two distinct SNP addresses at t5 level (≤5 SNP difference to at least one other case in the cluster, based on single linkage clustering) were selected to define an outbreakconfirmed case.…”
Section: Event Backgroundmentioning
confidence: 99%
“…Core genome positions that had a high-quality SNP (>90% consensus, minimum depth 10x, MQ >= 30) in at least one isolate were extracted and RaxML v8.2.8 [25] used to derive the maximum likelihood phylogeny of the isolates after first removing regions of the genome predicted to have undergone horizontal exchange using Gubbins v2.0.0 [26]. Hierarchical single linkage clustering was performed on the pairwise SNP difference between all isolates at various distance thresholds (Δ250, Δ100, Δ50, Δ25, Δ10, Δ5, Δ0) [27]. Genome-derived serotyping and AMR-conferring genes and SNPs was performed using the GeneFinder tool (https://github.com/phe-bioinformatics/gene_finder) [21,28].…”
Section: Whole Genome Sequencingmentioning
confidence: 99%