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- Publisher Website: 10.1093/bioadv/vbae030
- Scopus: eid_2-s2.0-85187941179
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Article: MetaQuad: shared informative variants discovery in metagenomic samples
Title | MetaQuad: shared informative variants discovery in metagenomic samples |
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Authors | |
Issue Date | 24-Feb-2024 |
Publisher | Oxford University Press |
Citation | Bioinformatics Advances, 2024, v. 4, n. 1 How to Cite? |
Abstract | Motivation: 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 Identifier | http://hdl.handle.net/10722/348646 |
DC Field | Value | Language |
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dc.contributor.author | Xu, Sheng | - |
dc.contributor.author | Morgan, Daniel C | - |
dc.contributor.author | Qian, Gordon | - |
dc.contributor.author | Huang, Yuanhua | - |
dc.contributor.author | Ho, Joshua WK | - |
dc.date.accessioned | 2024-10-11T00:31:08Z | - |
dc.date.available | 2024-10-11T00:31:08Z | - |
dc.date.issued | 2024-02-24 | - |
dc.identifier.citation | Bioinformatics Advances, 2024, v. 4, n. 1 | - |
dc.identifier.uri | http://hdl.handle.net/10722/348646 | - |
dc.description.abstract | Motivation: 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.language | eng | - |
dc.publisher | Oxford University Press | - |
dc.relation.ispartof | Bioinformatics Advances | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.title | MetaQuad: shared informative variants discovery in metagenomic samples | - |
dc.type | Article | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1093/bioadv/vbae030 | - |
dc.identifier.scopus | eid_2-s2.0-85187941179 | - |
dc.identifier.volume | 4 | - |
dc.identifier.issue | 1 | - |
dc.identifier.eissn | 2635-0041 | - |
dc.identifier.issnl | 2635-0041 | - |