Evidence map›Paper›PMID 42412834›Full record

ArticleBioinformatics (Oxford, England)2026

The gift of novelty: repeat-robust k-mer-based estimators of mutation rates.

Haonan Wu, Paul Medvedev

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Haonan WuDepartment of Computer Science and Engineering, The Pennsylvania State University, University Park, PA 16802, United States.
Paul MedvedevDepartment of Computer Science and Engineering, The Pennsylvania State University, University Park, PA 16802, United States.

Funding

Leveraging k-mer sketching statistics to enhance metagenomic methods and alignment algorithmsR01GM146462 · NIGMS · PENNSYLVANIA STATE UNIVERSITY, THE · PI Antonio Blanca Pimentel, David Koslicki · 2022 to 2026
$2.2M
National Science Foundation DBI2138585National Science Foundation OAC1931531NIGMS NIH HHS R01 GM146462NIH HHS R01GM146462
6 · The paper itself

Abstract

motivationEstimating mutation rates between evolutionarily related sequences is a central problem in molecular evolution. Due to the rapid expansion of datasets, modern methods avoid costly alignment and instead compare sketches of sets of constituent k-mers. While these methods perform well on many sequences, they are not robust to highly repetitive sequences such as centromeres.

resultsWe present three new estimators that are robust to the presence of repeats. The estimators are applicable in different settings, depending on whether count information is available from zero, one, or both sequences. We evaluate our estimators empirically using highly repetitive alpha satellite sequences. Each estimator performs best within its class, and our strongest estimator outperforms all other tested estimators. AVAILABILITY AND IMPLEMENTATION: Our software is open-source and freely available at https://github.com/medvedevgroup/Accurate_repeat-aware_kmer_based_estimator.

Indexed as

Mutation RateRepetitive Sequences, Nucleic AcidSequence Analysis, DNASoftwareAlgorithmsEvolution, Molecular

Identifiers

PMID42412834
PMCPMC13340239

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.