bronko: ultrafast, alignment-free detection of viral genome variation

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Abstract

As viral sequencing datasets continue to grow, traditional alignment-based variant calling pipelines are becoming computationally prohibitive. To address these challenges, we developed bronko , an ultrafast alignment-free framework for detecting viral variation directly from sequencing data. The novel computational approach implemented in bronko allows scaling to massive viral sequencing datasets and has three key components: i) a locality-sensitive bucketing function to rapidly identify single-nucleotide polymorphisms (SNPs) relative to reference(s), ii) a direct k-mer count psuedo-mapping approach that approximates a pileup without alignment, and iii) a streaming-based sliding window outlier test to estimate baseline noise across the genome and precisely differentiate real minor variants from noise. Together, these components yield near-linear computational complexity with respect to sequencing depth, enabling bronko to process thousands of viral samples rapidly on modest hardware. Our results are threefold: 1) On simulated amplicon sequencing, bronko recovers variants with higher precision and comparable recall to existing tools while running up to one to three orders of magnitude faster; 2) bronko generates sequence alignments directly from sequencing data, with SNP content similar to that of whole-genome alignment while also running in a fraction of the time, and 3) applying bronko to longitudinal sequencing data from chronically infected SARS-CoV-2 patients revealed consistent patterns of intrahost diversification and adaptive mutations over time. Altogether, these results demonstrate bronko 's potential as a scalable tool for large-scale viral genomic analyses, overcoming longstanding computational barriers for intrahost and interhost characterization of viral variation.
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Abstract As viral sequencing datasets continue to grow, traditional alignment-based variant calling pipelines are becoming computationally prohibitive. To address these challenges, we developed bronko, an ultrafast alignment-free framework for detecting viral variation directly from sequencing data. The novel computational approach implemented in bronko allows scaling to massive viral sequencing datasets and has three key components: i) a locality-sensitive bucketing function to rapidly identify single-nucleotide polymorphisms (SNPs) relative to reference(s), ii) a direct k-mer count pseudo-mapping approach that approximates a pileup without alignment, and iii) a streaming-based sliding window outlier test to estimate baseline noise across the genome and precisely differentiate real minor variants from noise. Together, these components yield near-linear computational complexity with respect to sequencing depth, enabling bronko to process thousands of viral samples rapidly on modest hardware. Our results are threefold: 1) On simulated amplicon sequencing, bronko recovers variants with higher precision and comparable recall to existing tools while running up to one to three orders of magnitude faster; 2) bronko generates sequence alignments directly from sequencing data, with SNP content similar to that of whole-genome alignment while also running in a fraction of the time, and 3) applying bronko to longitudinal sequencing data from chronically infected SARS-CoV-2 patients revealed consistent patterns of intrahost diversification and adaptive mutations over time. Altogether, these results demonstrate bronko’s potential as a scalable tool for large-scale viral genomic analyses, overcoming longstanding computational barriers for intrahost and interhost characterization of viral variation. Availability bronko is implemented in Rust and publicly available at https://github.com/treangenlab/bronko or via conda at https://anaconda.org/channels/bioconda/packages/bronko/overview. All results, evaluations, and other code used in this study are available at https://github.com/treangenlab/bronko-test. Competing Interest Statement The authors have declared no competing interest. Footnotes Supplementary updated with new benchmarking results, data descriptions; minor updates to text in both results and discussion; added new funding source and acknowledgements

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last seen: 2026-05-20T01:45:00.602351+00:00