Computational benchmark demonstrates superior sequence analysis performance across diverse genomic datasets, indicating the utility of nonlinear algebraic representations in genomics.
Despite the availability of various sequence analysis models, comparative genomic analysis remains a challenge in genomics, genetics, and phylogenetics. Commutative algebra, a fundamental tool in algebraic geometry and number theory, has rarely been used in data and biological sciences. In this study, we introduce commutative algebra k-mer representations as a nonlinear algebraic framework for analyzing genomic sequences. This representation bridges commutative algebra, algebraic topology, combinatorics, and machine learning to establish a mathematical framework for comparative genomic analysis. We evaluate its effectiveness on three tasks including genetic variant classification, phylogenetic tree reconstruction, and viral classification, typically requiring alignment-based, alignment-free, and machine-learning approaches, respectively. In this work, we show that commutative algebra k-mer representations outperform five state-of-the-art sequence analysis methods across twelve primary datasets, with two additional supplementary fragment-placement benchmarks, especially in viral classification, and maintain relatively stable predictive accuracy as dataset size increases, underscoring scalability and robustness. Comparative genomic analysis remains a fundamental challenge in genomics, genetics and phylogenetics, motivating the development of new mathematical frameworks for sequence comparison. The authors introduce a commutative algebra k-mer representation that integrates concepts from algebra, topology, combinatorics and machine learning, and evaluate its application to genetic variant classification, phylogenetic tree reconstruction and viral classification.
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Suwayyid et al. (2026) studied this question.
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