Please use this identifier to cite or link to this item: https://doi.org/10.1186/1471-2164-15-S10-S10
DC FieldValue
dc.titleGWAMAR: Genome-wide assessment of mutations associated with drug resistance in bacteria
dc.contributor.authorWozniak, M
dc.contributor.authorTiuryn, J
dc.contributor.authorWong, L
dc.date.accessioned2020-10-27T11:10:54Z
dc.date.available2020-10-27T11:10:54Z
dc.date.issued2014
dc.identifier.citationWozniak, 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
dc.identifier.issn14712164
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181518
dc.description.abstractBackground: 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.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectciprofloxacin
dc.subjectethambutol
dc.subjectisoniazid
dc.subjectlevofloxacin
dc.subjectmoxifloxacin
dc.subjectofloxacin
dc.subjectpyrazinamide
dc.subjectquinoline derived antiinfective agent
dc.subjectrifampicin
dc.subjectstreptomycin
dc.subjectantibiotic resistance
dc.subjectArticle
dc.subjectbacterial genome
dc.subjectbacterial strain
dc.subjectmultigene family
dc.subjectMycobacterium tuberculosis
dc.subjectnonhuman
dc.subjectpoint mutation
dc.subjectalgorithm
dc.subjectbacterial genome
dc.subjectcomparative study
dc.subjectcomputer program
dc.subjectgenetic association
dc.subjectgenetic database
dc.subjectgenetics
dc.subjectnucleotide sequence
dc.subjectphylogeny
dc.subjectprocedures
dc.subjectstatistical model
dc.subjectAlgorithms
dc.subjectDatabases, Genetic
dc.subjectDNA Mutational Analysis
dc.subjectDrug Resistance, Bacterial
dc.subjectGenome, Bacterial
dc.subjectGenome-Wide Association Study
dc.subjectModels, Statistical
dc.subjectMultigene Family
dc.subjectMycobacterium tuberculosis
dc.subjectPhylogeny
dc.subjectPoint Mutation
dc.subjectSoftware
dc.typeArticle
dc.contributor.departmentINSTITUTE OF SYSTEMS SCIENCE
dc.description.doi10.1186/1471-2164-15-S10-S10
dc.description.sourcetitleBMC Genomics
dc.description.volume15
dc.description.pageS10
Appears in Collections:Elements
Staff Publications

Show simple item record
Files in This Item:
File Description SizeFormatAccess SettingsVersion 
10_1186_1471-2164-15-S10-S10.pdf1.6 MBAdobe PDF

OPEN

NoneView/Download

Google ScholarTM

Check

Altmetric


This item is licensed under a Creative Commons License Creative Commons