Evidence map›Paper›PMID 37982752›Full record

ArticleBioinformatics (Oxford, England)2023

Snapper: high-sensitive detection of methylation motifs based on Oxford Nanopore reads.

Dmitry N Konanov, Vladislav V Babenko, Aleksandra M Belova, Arina G Madan, Daria I Boldyreva, Oksana E Glushenko, Ivan O Butenko, Dmitry E Fedorov, Alexander I Manolov, Danil V Krivonos and 3 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.6field-weighted citation impact, top 29% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Dmitry N KonanovResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.ORCID 0000-0002-1217-9234
Vladislav V BabenkoFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Aleksandra M BelovaFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Arina G MadanFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Daria I BoldyrevaFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Oksana E GlushenkoResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Ivan O ButenkoResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Dmitry E FedorovResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Alexander I ManolovResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Danil V KrivonosResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Vassilii N LazarevFederal Research and Clinical Center of Physical-Chemical Medicine, Federal Medical Biological Agency, Moscow 119435, Russia.
Vadim M GovorunResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
Elena N IlinaResearch Institute for Systems Biology and Medicine, Moscow 117246, Russia.
InSysBio (Russia) · RUFederal Medical-Biological Agency · RUMoscow Institute of Physics and Technology · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationThe Oxford Nanopore technology has a great potential for the analysis of methylated motifs in genomes, including whole-genome methylome profiling. However, we found that there are no methylation motifs detection algorithms, which would be sensitive enough and return deterministic results. Thus, the MEME suit does not extract all Helicobacter pylori methylation sites de novo even using the iterative approach implemented in the most up-to-date methylation analysis tool Nanodisco.

resultsWe present Snapper, a new highly sensitive approach, to extract methylation motif sequences based on a greedy motif selection algorithm. Snapper does not require manual control during the enrichment process and has enrichment sensitivity higher than MEME coupled with Tombo or Nanodisco instruments that was demonstrated on H.pylori strain J99 studied earlier by the PacBio technology and on four external datasets representing different bacterial species. We used Snapper to characterize the total methylome of a new H.pylori strain A45. At least four methylation sites that have not been described for H.pylori earlier were revealed. We experimentally confirmed the presence of a new CCAG-specific methyltransferase and inferred a gene encoding a new CCAAK-specific methyltransferase. AVAILABILITY AND IMPLEMENTATION: Snapper is implemented using Python and is freely available as a pip package named "snapper-ont." Also, Snapper and the demo dataset are available in Zenodo (10.5281/zenodo.10117651).

Indexed as

Genome, BacterialNanoporesAlgorithmsDNA MethylationHigh-Throughput Nucleotide SequencingMethyltransferasesSequence Analysis, DNAMethyltransferases

Identifiers

PMID37982752
PMCPMC10689673
OpenAlexW4388822389

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.