MEGARes 2.0
MEGARes 2.0 provides a curated database and hierarchical ontology for identifying and quantifying antimicrobial, metal, and biocide resistance genes in high-throughput sequencing metagenomic datasets.
Key Features:
- Curated Resistance Gene Database: Contains approximately 7,868 curated gene accessions associated with antimicrobial, metal, and biocide resistance.
- Hierarchical Ontology Framework: Organizes resistance genes using an acyclic hierarchical ontology consisting of four compound types, 57 resistance classes, 220 resistance mechanisms, and 1,345 gene groups.
- Population-Level Resistome Analysis: Enables hierarchical count-based statistical analysis of resistance genes across microbial communities.
- Integration with AmrPlusPlus 2.0: Supports identification and quantification of antimicrobial resistance gene accessions in metagenomic datasets through the AmrPlusPlus (version 2.0) analysis pipeline.
Scientific Applications:
- Metagenomic Resistome Profiling: Detects and quantifies antimicrobial, metal, and biocide resistance genes in high-throughput sequencing datasets.
- Antimicrobial Resistance Surveillance: Supports epidemiological investigation of resistance gene distribution across microbial communities.
- Resistance Gene Classification: Provides structured annotations for statistical modeling and classifier development in antimicrobial resistance research.
Methodology:
MEGARes 2.0 analyzes high-throughput sequencing metagenomic data by mapping resistance gene sequences to a curated database organized within an acyclic hierarchical ontology and integrates with the AmrPlusPlus 2.0 pipeline to identify and quantify resistance gene accessions.
Topics
Details
- Tool Type:
- web application
- Added:
- 1/14/2020
- Last Updated:
- 11/24/2024
Operations
Publications
Doster E, Lakin SM, Dean CJ, Wolfe C, Young JG, Boucher C, Belk KE, Noyes NR, Morley PS. MEGARes 2.0: a database for classification of antimicrobial drug, biocide and metal resistance determinants in metagenomic sequence data. Nucleic Acids Research. 2019;48(D1):D561-D569. doi:10.1093/nar/gkz1010. PMID:31722416. PMCID:PMC7145535.