Evidence map›Paper›PMID 41357306›Full record

ArticleBioinformatics advances2025

Snappy: fast identification of DNA methylation motifs based on oxford nanopore reads.

Dmitry N Konanov, Danil V Krivonos, Vladislav V Babenko, Elena N Ilina

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Article in Bioinformatics advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
–field-weighted citation impact
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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Dmitry N KonanovLaboratory of Mathematical Biology and Bioinformatics, Research Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, 117246, Russia.ORCID https://orcid.org/0000-0002-1217-9234
Danil V KrivonosLaboratory of Mathematical Biology and Bioinformatics, Research Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, 117246, Russia.ORCID https://orcid.org/0000-0002-3851-5873
Vladislav V BabenkoDepartment of Biomedicine and Genomics, Lopukhin Federal Research and Clinical Center of Physical-Chemical Medicine of Federal Medical Biological Agency, Moscow, 119435, Russia.
Elena N IlinaLaboratory of Mathematical Biology and Bioinformatics, Research Institute for System Biology and Medicine of Rospotrebnadzor, Moscow, 117246, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Motivation: Nowadays, DNA methylation in bacteria is studied mainly using single-molecule sequencing technologies like PacBio and Oxford Nanopore. In nanopore sequencing, calling of methylated positions is provided by special models implemented directly in basecallers. Prokaryotic DNA methyltransferases are site-specific enzymes, which catalyze methylation in specific methylation motifs. Inference of these motifs is usually performed using third party software like MEME providing classical motif enrichment based only on sequence data. However, currently used motif enrichment algorithms rely only on sequence data, and do not use additional base modification information provided by the basecaller. Results: Herein, we present a new tool Snappy, which is actually rethinking of the original Snapper algorithm but does not use any enrichment heuristics and does not require control sample sequencing. Snappy combines basecalling data processing with a new graph-based enrichment algorithm, thus significantly enhancing the enrichment sensitivity and accuracy. The versatility of the method was shown on both our and external data, representing different bacterial species with complex and simple methylome. Availability and implementation: Source code and documentation is hosted on GitHub (https://github.com/DNKonanov/ont-snappy) and Zenodo (zenodo.org/records/16731817). For accessibility, Snappy is installable from PyPi using "pip install ont-snappy" command.

Identifiers

PMID41357306
PMCPMC12679398

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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.