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Article: MetaQuad: shared informative variants discovery in metagenomic samples

TitleMetaQuad: shared informative variants discovery in metagenomic samples
Authors
Issue Date24-Feb-2024
PublisherOxford University Press
Citation
Bioinformatics Advances, 2024, v. 4, n. 1 How to Cite?
AbstractMotivation: Strain-level analysis of metagenomic data has garnered significant interest in recent years. Microbial single nucleotide polymorphisms (SNPs) are genomic variants that can reflect strain-level differences within a microbial species. The diversity and emergence of SNPs in microbial genomes may reveal evolutionary history and environmental adaptation in microbial populations. However, efficient discovery of shared polymorphic variants in a large collection metagenomic samples remains a computational challenge. Results: MetaQuad utilizes a density-based clustering technique to effectively distinguish between shared variants and non-polymorphic sites using shotgun metagenomic data. Empirical comparisons with other state-of-the-art methods show that MetaQuad significantly reduces the number of false positive SNPs without greatly affecting the true positive rate. We used MetaQuad to identify antibiotic-associated variants in patients who underwent Helicobacter pylori eradication therapy. MetaQuad detected 7591 variants across 529 antibiotic resistance genes. The nucleotide diversity of some genes is increased 6 weeks after antibiotic treatment, potentially indicating the role of these genes in specific antibiotic treatments. Availability and implementation: MetaQuad is an open-source Python package available via https://github.com/holab-hku/MetaQuad.
Persistent Identifierhttp://hdl.handle.net/10722/348646

 

DC FieldValueLanguage
dc.contributor.authorXu, Sheng-
dc.contributor.authorMorgan, Daniel C-
dc.contributor.authorQian, Gordon-
dc.contributor.authorHuang, Yuanhua-
dc.contributor.authorHo, Joshua WK-
dc.date.accessioned2024-10-11T00:31:08Z-
dc.date.available2024-10-11T00:31:08Z-
dc.date.issued2024-02-24-
dc.identifier.citationBioinformatics Advances, 2024, v. 4, n. 1-
dc.identifier.urihttp://hdl.handle.net/10722/348646-
dc.description.abstractMotivation: Strain-level analysis of metagenomic data has garnered significant interest in recent years. Microbial single nucleotide polymorphisms (SNPs) are genomic variants that can reflect strain-level differences within a microbial species. The diversity and emergence of SNPs in microbial genomes may reveal evolutionary history and environmental adaptation in microbial populations. However, efficient discovery of shared polymorphic variants in a large collection metagenomic samples remains a computational challenge. Results: MetaQuad utilizes a density-based clustering technique to effectively distinguish between shared variants and non-polymorphic sites using shotgun metagenomic data. Empirical comparisons with other state-of-the-art methods show that MetaQuad significantly reduces the number of false positive SNPs without greatly affecting the true positive rate. We used MetaQuad to identify antibiotic-associated variants in patients who underwent Helicobacter pylori eradication therapy. MetaQuad detected 7591 variants across 529 antibiotic resistance genes. The nucleotide diversity of some genes is increased 6 weeks after antibiotic treatment, potentially indicating the role of these genes in specific antibiotic treatments. Availability and implementation: MetaQuad is an open-source Python package available via https://github.com/holab-hku/MetaQuad.-
dc.languageeng-
dc.publisherOxford University Press-
dc.relation.ispartofBioinformatics Advances-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleMetaQuad: shared informative variants discovery in metagenomic samples-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1093/bioadv/vbae030-
dc.identifier.scopuseid_2-s2.0-85187941179-
dc.identifier.volume4-
dc.identifier.issue1-
dc.identifier.eissn2635-0041-
dc.identifier.issnl2635-0041-

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