Deployable high-fidelity metagenome binning at scale with QuickBin
Reconstructing genomes from metagenomic assemblies is foundational to microbiome research, yet binning faces a persistent trade-off between fidelity and throughput. Many high-accuracy methods rely on GPU-intensive workflows, marker-gene postprocessing, or heavy computational resources, limiting reproducible use at scale. Here, we present QuickBin, a CPU-native, marker-free binning algorithm designed to recover near-complete, ultra-low-contamination metagenome-assembled genomes (MAGs) efficiently. QuickBin pairs a GC-coverage spatial index (BinMap) with an early-exit Oracle cascade of similarity tests (scalar composition/coverage filters and SIMD-accelerated k-mer comparisons), reserving a compact neural network exclusively for ambiguous merges. Across synthetic communities, evaluated by marker-based and contig-origin ground truth, QuickBin maximizes high-fidelity sequence recovery. In benchmarking 297 diverse real metagenomes, QuickBin completed all runs, recovering more high-quality MAGs (≥95% completeness, ≤1% contamination) than resource-intensive alternatives that frequently failed. QuickBin provides a practical path to reproducible, genome-resolved metagenomics at scale for downstream comparative analyses. Open-source at: https://github.com/bbushnell/BBTools .
Authors
- Juan C. Villada (ORCID: https://orcid.org/0000-0003-2216-4279)
- Brian Bushnell (ORCID: https://orcid.org/0000-0002-8140-0131)
Institutions
- Lawrence Berkeley National Laboratory (US)
- Joint Genome Institute (US)
Publication Details
- Journal
- Communications Biology
- Published
- 2026-08-25
- DOI
- https://doi.org/10.1038/s42003-026-10782-z
- Primary Topic
- Genomics and Phylogenetic Studies
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- U.S. Department of Energy
- Joint Genome Institute
- National Energy Research Scientific Computing Center
- Office of Science
- Lawrence Berkeley National Laboratory