Search bioRxiv⌕ Search

bioRxiv · 10.64898/2026.03.11.709163

GradeBins: a comprehensive framework to augment metagenomic bin quality control

Abstract

1.Metagenomic binning and single-cell assembly produce draft genomes whose completeness and contamination vary with experimental and computational choices. Comparing whole bin sets remains difficult because most quality assessment tools report per-bin metrics and operate either with ground truth labels or with inference estimates. GradeBins evaluates complete bin sets under two execution modes while producing matched per-bin and bin-set summaries. For real metagenomes, inference mode integrates bin statistics, mapping depth, taxonomy, and external quality estimates from tools such as CheckM2 and EukCC to standardize per-bin and bin-set quality reporting across Bacteria, Archaea, and Eukaryotes. For synthetic or otherwise labeled datasets, ground truth mode computes base-resolved completeness, contamination, and misbinning from labeled contigs or CAMI mappings, enabling objective benchmarking of binners, parameter choices, and experimental conditions, and calibration of inference-based estimates. Across synthetic metagenomes of 10, 50, 100, 500 and 1,000 Bacteria and Archaea, and a mixed metagenome containing also Eukaryotes, GradeBins separated binner and parameter effects using Total Score and a quality-weighted bin count, together with quality tier distributions, recovery fractions, and label-aware diagnostics. Inference-mode completeness generally tracked ground truth, whereas contamination and clean-bin rates showed mode-dependent shifts that were most pronounced in the mixed community. GradeBins added low overhead in these benchmarks, with peak memory below 8 GB and runtimes typically below 30 seconds. GradeBins enables reproducible protocol comparison, regression testing, and consistent quality reporting for genome-resolved metagenomics in both benchmarking and real-data settings. The full software package is open-source and available for download at https://bbmap.org/tools/gradebins.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Bushnell, B., Bowers, R. M., Villada, J. C.. 2026-03-12. GradeBins: a comprehensive framework to augment metagenomic bin quality control. https://doi.org/10.64898/2026.03.11.709163

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

A conserved cysteine-histidine-glutamate metal site identifies DUF501 (Rv1025), an essential uncharacterised protein family of Mycobacterium tuberculosis, as a candidate metalloenzyme and drug target

A substantial fraction of the Mycobacterium tuberculosis proteome remains functionally uncharacterised. Rv1025, a 155-residue protein carrying the domain of unknown function DUF501 (Pfam PF04417), is essential by transposon mutagenesis and vulnerable by CRISPR interference, an attractive but neglected drug target, yet has never been functionally described. The family (4,370 proteins, no Gene Ontology term, no solved structure) is uncharacterised across all organisms and essential in three Actinobacterial genera. A Foldseek search of the AlphaFold model against complete structural databases finds no significant homolog, indicating a novel fold. The operon eno-divIC-Rv1025-ppx2 is conserved across the Actinobacteria phylum, yet AlphaFold-Multimer finds no direct complex between Rv1025 and its neighbour DivIC. Instead, conservation across 8,700 homologous sequences reveals a near-invariant Cys113-His115-Glu59 cluster forming a pocket. Holo AlphaFold3 predictions with Zn, Fe and Mn confidently place a divalent metal on this triad at 2.25-2.47 A; mutating the triad relocates the metal, and an independent backbone-geometry predictor recovers the same site, confirming specificity. The triad is universal across the family: present in all 1,472 near-complete bacterial sequences of the Pfam alignment, with no non-conservative substitution among the 2,228 sequences examined, a defining feature of bacterial DUF501 rather than a mycobacterial peculiarity. We propose that DUF501 is a metal-binding protein and candidate metalloenzyme, the first functional hypothesis for this family, whose conserved, essential metal pocket is a promising drug target. As the predictions build on a conservation-defined site within a fully computational study, they are supportive rather than proof of metal occupancy and warrant experimental validation.

microbiology↗

Mycoplasmal endosymbionts of Trichomonas vaginalis are associated with reduced risk for Chlamydia trachomatis endometrial infection in asymptomatic, coinfected, women.

Trichomonas vaginalis is a protozoan parasite that causes trichomoniasis, the most common curable non-viral sexually transmitted infection, and Chlamydia trachomatis is a bacterial pathogen that can ascend to the upper genital tract and cause pelvic inflammatory disease, infertility, and ectopic pregnancy. T. vaginalis harbors bacterial endosymbionts, including Candidatus Malacoplasma girerdii, an obligate symbiont, and Metamycoplasma hominis, which can live freely or symbiotically. In a 16S rRNA sequencing study of the cervicovaginal microbiome of women at high risk for chlamydial infection, Ca. M. girerdii abundance was one of 13 features predicting lack of chlamydial spread to the endometrium, despite no direct association between T. vaginalis infection and reduced chlamydial ascension. Investigating the relationship between these microorganisms further, we found that T. vaginalis vaginal abundance correlated positively with chlamydial burden in women whose infection was confined to the cervix, while a nonsignificant inverse relationship was seen in women with endometrial spread. Among participants with high chlamydial burden, Ca. M. girerdii was detected exclusively in women without endometrial infection. Both endosymbionts trended toward more frequent detection, and higher abundance, in coinfected women without endometrial spread, while M. hominis abundance correlated strongly with T. vaginalis burden in this group. These findings suggest that mycoplasmal endosymbionts of T. vaginalis, rather than T. vaginalis itself, are microbial factors limiting chlamydial ascension, and point to a three-way interaction between parasite, endosymbiont, and bacterial pathogen that shapes upper genital tract C. trachomatis infection risk.

microbiology↗

Understanding the physiological alterations of Vibrio cholerae upon exposure to L-ascorbic acid

The scourge of cholera remains a major global public health threat. It affects up to 4 million people worldwide and causes tens of thousands of deaths each year. The disease is experiencing a concerning resurgence in many parts of Africa, the Middle East, and Asia. To effectively tackle cholera and circumvent rising antimicrobial resistance, targeted biological and preventive approaches, complementing traditional rehydration, are urgently needed. In this regard, our group has demonstrated the efficacy of L-ascorbic acid in controlling the growth and pathogenesis of Vibrio cholerae in vitro. The present work further provides a mechanistic elucidation of the L-ascorbic acid-mediated physiological changes in V. cholerae and also bolsters such a non-antibiotic approach to control cholera.

microbiology↗