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Taboada, E. N.

Publications and source records attributed to Taboada, E. N..

4 recordsLinked to original sources

MMMVI: Detecting SARS-CoV-2 Variants of Concern in Metagenomic Samples

MotivationSARS-CoV-2 is the causative agent of the COVID-19 pandemic. Variants of Concern (VOCs) and Variants of Interest (VOIs) are lineages that represent a greater risk to public health, and can be differentiated from the wildtype virus based on unique profiles of signature mutations. Metagenomic sequence analysis of wastewater represents an emerging form of surveillance that can capture early signal for these variants in a community prior to detection through public health testing or genomic surveillance activities. However, because multiple viral genomes are likely to be present in a metagenomic sample, additional analytical scrutiny of the sequencing reads beyond variant calling is needed to increase confidence in diagnostic determinations. ResultsWhere multiple signature mutations are present on a given read, they can be used as enhanced biomarkers to confirm the presence of a VOC/VOI in the sample. We have developed MMMVI, a tool to aggregate and report on the likely presence of a VOC/VOI in a set of metagenomic reads based on the detection of reads bearing multiple signature mutations. AvailabilityMMMVI is implemented in Python, and is available under the MIT licence from https://github.com/dorbarker/voc-identify/ Contactdillon.barker@canada.ca

bioinformatics↗

Rapid and accurate SNP genotyping of clonal bacterial pathogens with BioHansel

BioHansel performs high-resolution genotyping of bacterial isolates by identifying phylogenetically informative single nucleotide polymorphisms (SNPs), also known as canonical SNPs, in whole genome sequencing (WGS) data. The application uses a fast k-mer matching algorithm to map pathogen WGS data to canonical SNPs contained in hierarchically structured schemas and assigns genotypes based on the detected SNP profile. Using modest computing resources, BioHansel efficiently types isolates from raw sequence reads or assembled contigs in a matter of seconds, making it attractive for use by public health, food safety, environmental, and agricultural authorities that wish to apply WGS methodologies for their surveillance, diagnostics, and research programs. BioHansel currently provides canonical SNP genotyping schemas for four prevalent Salmonella serovars--Typhi, Typhimurium, Enteritidis and Heidelberg--as well as a schema for Mycobacterium tuberculosis. Users can also supply their own schemas for genotyping other organisms. BioHansels quality assurance system assesses the validity of the genotyping results and can identify low quality data, contaminated datasets, and misidentified organisms. BioHansel is targeted to support surveillance, source attribution, risk assessment, diagnostics, and rapid screening for public health purposes, such as product recalls. BioHansel is an open source application with packages available for PyPI, Conda, and the Galaxy workflow manager. In summary, BioHansel performs efficient, rapid, accurate, and high-resolution classification of bacterial genomes from sequence reads or assembled contigs on standard computing hardware. BioHansel is suitable for use as a general research tool as well as in fully operationalized WGS workflows at the front lines of infectious disease surveillance, diagnostics, and outbreak investigation and response. Impact statementPublic health, food safety, environmental, and agricultural authorities are currently engaged in a global effort to incorporate whole genome sequencing technologies into their infectious disease research, surveillance, and outbreak investigation programs. Its widespread adoption, however, has been impeded by two major obstacles: the need for high performance computing to generate results and the expert knowledge required to interpret and communicate those results. BioHansel addresses these limitations by rapidly genotyping pathogens from whole genome sequence data in an accurate, simple, familiar, and easily sharable manner using standard computing resources. BioHansel provides a compact and readily interpretable genotype based on canonical SNP genotyping schemas. BioHansels genotyping nomenclature encodes the pathogens position in its population structure, which simplifies and facilitates its comparison with actively circulating strains and historical strains. The genotyping information provided by BioHansel can identify points of intervention to prevent the spread of pathogenic bacteria, screen for the presence of priority pathogens, and perform source attribution and risk assessment. Thus, BioHansel serves as a readily accessible and powerful WGS method, implementable on a laptop, for genotyping pathogens to detect, monitor, and control the emergence and spread of infectious disease through surveillance, screening, diagnostics, and outbreak investigation and response activities. Data summaryBioHansel is a Python 3 application available as PyPI, Conda Galaxy Tool Shed packages. It is an open source application distributed under the Apache License, Version 2.0. Source code is available at https://github.com/phac-nml/biohansel. The BioHansel user guide is available at https://bio-hansel.readthedocs.io/en/readthedocs/. Supplementary Materials are available at https://github.com/phac-nml/biohansel-manuscript-supplementary-data. The authors confirm all supporting data, code and protocols have been provided within the article or through supplementary data files.

bioinformatics↗

The Integrated Rapid Infectious Disease Analysis (IRIDA) Platform

Whole genome sequencing (WGS) is a powerful tool for public health infectious disease investigations owing to its higher resolution, greater efficiency, and cost-effectiveness over traditional genotyping methods. Implementation of WGS in routine public health microbiology laboratories is impeded by a lack of user-friendly automated and semi-automated pipelines, restrictive jurisdictional data sharing policies, and the proliferation of non-interoperable analytical and reporting systems. To address these issues, we developed the Integrated Rapid Infectious Disease Analysis (IRIDA) platform (irida.ca), a user-friendly, decentralized, open-source bioinformatics and analytical web platform to support real-time infectious disease outbreak investigations using WGS data. Instances can be independently installed on local high-performance computing infrastructure, enabling private and secure data management and analyses according to organizational policies and governance. IRIDAs data management capabilities enable secure upload, storage and sharing of all WGS data and metadata. The core platform currently includes pipelines for quality control, assembly, annotation, variant detection, phylogenetic analysis, in silico serotyping, multi-locus sequence typing, and genome distance calculation. Analysis pipeline results can be visualized within the platform through dynamic line lists and integrated phylogenomic clustering for research and discovery, and for enhancing decision-making support and hypothesis generation in epidemiological investigations. Communication and data exchange between instances are provided through customizable access controls. IRIDA complements centralized systems, empowering local analytics and visualizations for genomics-based microbial pathogen investigations. IRIDA is currently transforming the Canadian public health ecosystem and is freely available at https://github.com/phac-nml/irida and www.irida.ca.\n\nImpact StatementWhole genome sequencing (WGS) is revolutionizing infectious disease analysis and surveillance due to its cost effectiveness, utility, and improved analytical power. To date, no \"one-size-fits-all\" genomics platform has been universally adopted, owing to differences in national (and regional) health information systems, data sharing policies, computational infrastructures, lack of interoperability and prohibitive costs. The Integrated Rapid Infectious Disease Analysis (IRIDA) platform is a user-friendly, decentralized, open-source bioinformatics and analytical web platform developed to support real-time infectious disease outbreak investigations using WGS data. IRIDA empowers public health, regulatory and clinical microbiology laboratory personnel to better incorporate WGS technology into routine operations by shielding them from the computational and analytical complexities of big data genomics. IRIDA is now routinely used as part of a validated suite of tools to support outbreak investigations in Canada. While IRIDA was designed to serve the needs of the Canadian public health system, it is generally applicable to any public health and multi-jurisdictional environment. IRIDA enables localized analyses but provides mechanisms and standard outputs to enable data sharing. This approach can help overcome pervasive challenges in real-time global infectious disease surveillance, investigation and control, resulting in faster responses, and ultimately, better public health outcomes.\n\nDATA SUMMARYO_LIData used to generate some of the figures in this manuscript can be found in the NCBI BioProject PRJNA305824.\nC_LI

bioinformatics↗

Rapid Identification of Stable Clusters in Bacterial Populations Using the Adjusted Wallace Coefficient

Whole-genome sequencing (WGS) of microbial pathogens has become an essential part of modern epidemiological investigations. Although WGS data can be analyzed using a number of different approaches, such as traditional phylogenetic methods, a critical requirement for global systems for pathogen surveillance is the development of approaches for transforming sequence data into WGS-based subtypes, which creates a nomenclature that describes their higher-order relationships to one another. To this end, subtype similarity thresholds are needed to define clusters of subtypes representing lineages of interest. WGS-based subtyping presents a challenge since both the addition of novel genome sequences and small adjustments in similarity thresholds can have a dramatic impact on cluster composition and stability. We present the Neighbourhood Adjusted Wallace Coefficient (nAWC), a method for evaluating cluster stability based on computing cluster concordance between neighbouring similarity thresholds. The nAWC can be used to identify areas in in which distance thresholds produce robust clusters. Using datasets from Salmonella enterica and Campylobacter jejuni, representing strongly and weakly clonal bacterial species respectively, we show that clusters generated using such thresholds are both stable and reflect basic units in their overall population structure. Our results suggest that the nAWC could be useful for defining robust clusters compatible with nomenclatures for global WGS-based surveillance networks, which require stable clusters to be defined that both harness the discriminatory power of WGS data while allowing for long-term tracking of strains of interest.

genomics↗