Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-15-S10-S10
Title: GWAMAR: Genome-wide assessment of mutations associated with drug resistance in bacteria
Authors: Wozniak, M
Tiuryn, J
Wong, L 
Keywords: ciprofloxacin
ethambutol
isoniazid
levofloxacin
moxifloxacin
ofloxacin
pyrazinamide
quinoline derived antiinfective agent
rifampicin
streptomycin
antibiotic resistance
Article
bacterial genome
bacterial strain
multigene family
Mycobacterium tuberculosis
nonhuman
point mutation
algorithm
bacterial genome
comparative study
computer program
genetic association
genetic database
genetics
nucleotide sequence
phylogeny
procedures
statistical model
Algorithms
Databases, Genetic
DNA Mutational Analysis
Drug Resistance, Bacterial
Genome, Bacterial
Genome-Wide Association Study
Models, Statistical
Multigene Family
Mycobacterium tuberculosis
Phylogeny
Point Mutation
Software
Issue Date: 2014
Citation: Wozniak, M, Tiuryn, J, Wong, L (2014). GWAMAR: Genome-wide assessment of mutations associated with drug resistance in bacteria. BMC Genomics 15 : S10. ScholarBank@NUS Repository. https://doi.org/10.1186/1471-2164-15-S10-S10
Rights: Attribution 4.0 International
Abstract: Background: Development of drug resistance in bacteria causes antibiotic therapies to be less effective and more costly. Moreover, our understanding of the process remains incomplete. One promising approach to improve our understanding of how resistance is being acquired is to use whole-genome comparative approaches for detection of drug resistance-associated mutations. Results: We present GWAMAR, a tool we have developed for detecting of drug resistance-associated mutations in bacteria through comparative analysis of whole-genome sequences. The pipeline of GWAMAR comprises several steps. First, for a set of closely related bacterial genomes, it employs eCAMBer to identify homologous gene families. Second, based on multiple alignments of the gene families, it identifies mutations among the strains of interest. Third, it calculates several statistics to identify which mutations are the most associated with drug resistance. Conclusions: Based on our analysis of two large datasets retrieved from publicly available data for M. tuberculosis, we identified a set of novel putative drug resistance-associated mutations. As a part of this work, we present also an application of our tool to detect putative compensatory mutations. © 2014 Wozniak et al.
Source Title: BMC Genomics
URI: https://scholarbank.nus.edu.sg/handle/10635/181518
ISSN: 14712164
DOI: 10.1186/1471-2164-15-S10-S10
Rights: Attribution 4.0 International
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