Evidence map›Paper›PMID 42711309›Full record

ArticleNature communications2026

CAKR: commutative algebra k-mer representations for genomics.

Faisal Suwayyid, Yuta Hozumi, Mushal Zia, JunJie Wee, Hongsong Feng, Guo-Wei Wei

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Faisal SuwayyidMathematics Department, King Fahd University of Petroleum and Minerals, Dhahran, Kingdom of Saudi Arabia.
Yuta HozumiDepartment of Mathematics, Michigan State University, East Lansing, MI, USA.
Mushal ZiaDepartment of Mathematics, Michigan State University, East Lansing, MI, USA.
JunJie WeeDepartment of Mathematics, Michigan State University, East Lansing, MI, USA.ORCID http://orcid.org/0000-0001-8444-3252
Hongsong FengDepartment of Mathematics and Statistics, University of North Carolina at Charlotte, Charlotte, NC, USA.
Guo-Wei WeiDepartment of Mathematics, Michigan State University, East Lansing, MI, USA. guowei.wei@uga.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

GenomicsAlgorithmsComputational BiologyMachine LearningPhylogenySequence Analysis, DNA

Identifiers

PMID42711309
PMCPMC13554176

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.