ResMiCo
ResMiCo identifies misassembled contigs in metagenome assemblies using a residual neural network to provide reference-free quality assessment of metagenome-assembled genomes.
Key Features:
- Residual neural network: Implements a residual neural network architecture tailored to detect misassembled contigs.
- Reference-free prediction: Operates without relying on reference genomes to identify misassemblies in assembled contigs.
- Robustness to taxonomic novelty: Demonstrates the ability to generalize to diverse and taxonomically novel genomic data and assembly methods.
- Benchmarking and accuracy: Shows substantial performance improvements over prior methods, which reported AUPRC not exceeding 0.57.
- Large-scale training dataset: Trained on a dataset of unprecedented size and complexity to support rigorous evaluation and model generalization.
- Assembly parameter optimization: Enables optimization of metagenome assembly hyperparameters with a focus on reducing misassemblies as well as improving contiguity.
Scientific Applications:
- Quality control: Applied to metagenomic studies to identify misassembled contigs and improve the fidelity of metagenome-assembled genomes.
- Methodology optimization: Used to inform adjustment of assembly parameters and workflows to reduce misassembly rates.
- Misassembly rate estimation: Applied to real-world datasets to estimate misassembly prevalence, reporting an average of approximately 7% misassembled contigs per metagenome in evaluations.
Methodology:
ResMiCo uses a residual neural network trained on a large, complex training dataset and evaluated via benchmarking metrics including AUPRC.
Topics
Details
- License:
- MIT
- Cost:
- Free of charge
- Tool Type:
- command-line tool
- Operating Systems:
- Mac, Linux, Windows
- Programming Languages:
- Python, C++
- Added:
- 1/3/2024
- Last Updated:
- 11/24/2024
Operations
Publications
Mineeva O, Danciu D, Schölkopf B, Ley RE, Rätsch G, Youngblut ND. ResMiCo: Increasing the quality of metagenome-assembled genomes with deep learning. PLOS Computational Biology. 2023;19(5):e1011001. doi:10.1371/journal.pcbi.1011001. PMID:37126495. PMCID:PMC10174551.
PMID: 37126495
PMCID: PMC10174551
Funding: - Eidgenössische Technische Hochschule Strategic Focus Area - Personalized Health and Related Technologies: project #106