ArticleBioinformatics (Oxford, England)2022
CMash: fast, multi-resolution estimation of k-mer-based Jaccard and containment indices.
Article in Bioinformatics (Oxford, England), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.
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12 citing papers in PubMed, 14 citations in OpenAlex.
- CamK-DB: A k-mer MinHash fingerprint database for reference-free genotyping of Camellia accessions.GigaScience · 2026Article
- HYMET: a hybrid metagenomic pipeline for accurate and efficient taxonomic classification.GigaScience · 2026Article
- Assessing Amplification Quality and Bias in MDA Methods Through Comparative Analysis of Short-Read Sequencing.Methods in molecular biology (Clifton, N.J.) · 2026Article
- Article
- MaxGeomHash: An Algorithm for Variable-Size Random Sampling of Distinct Elements.bioRxiv : the preprint server for biology · 2025Article
- Estimating similarity and distance using FracMinHash.Algorithms for molecular biology : AMB · 2025Article
- Taming large-scale genomic analyses via sparsified genomics.Nature communications · 2025Article
- Analysis of metagenomic data.Nature reviews. Methods primers · 2025Article
- GSearch: ultra-fast and scalable genome search by combining K-mer hashing with hierarchical navigable small world graphs.Nucleic acids research · 2024Article
- Metagenomic functional profiling: to sketch or not to sketch?Bioinformatics (Oxford, England) · 2024Article
- Cosine Similarity Estimation Using FracMinHash: Theoretical Analysis, Safety Conditions, and Implementation.bioRxiv : the preprint server for biology · 2024Article
- Employing bimodal representations to predict DNA bendability within a self-supervised pre-trained framework.Nucleic acids research · 2024Article
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2 authors at 1 institution in 1 country.
Funding
Abstract
motivationK-mer-based methods are used ubiquitously in the field of computational biology. However, determining the optimal value of k for a specific application often remains heuristic. Simply reconstructing a new k-mer set with another k-mer size is computationally expensive, especially in metagenomic analysis where datasets are large. Here, we introduce a hashing-based technique that leverages a kind of bottom-m sketch as well as a k-mer ternary search tree (KTST) to obtain k-mer-based similarity estimates for a range of k values. By truncating k-mers stored in a pre-built KTST with a large k=kmax value, we can simultaneously obtain k-mer-based estimates for all k values up to kmax. This truncation approach circumvents the reconstruction of new k-mer sets when changing k values, making analysis more time and space-efficient.
resultsWe derived the theoretical expression of the bias factor due to truncation. And we showed that the biases are negligible in practice: when using a KTST to estimate the containment index between a RefSeq-based microbial reference database and simulated metagenome data for 10 values of k, the running time was close to 10× faster compared to a classic MinHash approach while using less than one-fifth the space to store the data structure. AVAILABILITY AND IMPLEMENTATION: A python implementation of this method, CMash, is available at https://github.com/dkoslicki/CMash. The reproduction of all experiments presented herein can be accessed via https://github.com/KoslickiLab/CMASH-reproducibles. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
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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.