Evidence map›Paper›PMID 39710838›Full record

ArticleBioinformatics (Oxford, England)2024

End-to-end simulation of nanopore sequencing signals with feed-forward transformers.

Denis Beslic, Martin Kucklick, Susanne Engelmann, Stephan Fuchs, Bernhard Y Renard, Nils Körber

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Article in Bioinformatics (Oxford, England), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Denis BeslicCentre for Artificial Intelligence in Public Health Research, Robert Koch Institute, Berlin 13353, Germany.ORCID 0000-0001-6346-7896
Martin KucklickInstitute for Microbiology, Technical University of Braunschweig, Braunschweig 38106, Germany.ORCID 0000-0002-7289-3915
Susanne EngelmannInstitute for Microbiology, Technical University of Braunschweig, Braunschweig 38106, Germany.ORCID 0000-0002-1201-3488
Stephan FuchsGenome Competence Center, Robert Koch Institute, Berlin 13353, Germany.ORCID 0000-0002-1338-2699
Bernhard Y RenardData Analytics and Computational Statistics, Hasso Plattner Institute, Digital Engineering Faculty, University of Potsdam, Potsdam 14482, Germany.ORCID 0000-0003-4589-9809
Nils KörberCentre for Artificial Intelligence in Public Health Research, Robert Koch Institute, Berlin 13353, Germany.ORCID 0009-0003-2506-4297

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

motivationNanopore sequencing represents a significant advancement in genomics, enabling direct long-read DNA sequencing at the single-molecule level. Accurate simulation of nanopore sequencing signals from nucleotide sequences is crucial for method development and for complementing experimental data. Most existing approaches rely on predefined statistical models, which may not adequately capture the properties of experimental signal data. Furthermore, these simulators were developed for earlier versions of nanopore chemistry, which limits their applicability and adaptability to the latest flow cell data.

resultsTo enhance the quality of artificial signals, we introduce seq2squiggle, a novel transformer-based, non-autoregressive model designed to generate nanopore sequencing signals from nucleotide sequences. Unlike existing simulators that rely on static k-mer models, our approach learns sequential contextual information from segmented signal data. We benchmark seq2squiggle against state-of-the-art simulators on real experimental R9.4.1 and R10.4.1 data, evaluating signal similarity, basecalling accuracy, and variant detection rates. Seq2squiggle consistently outperforms existing tools across multiple datasets, demonstrating superior similarity to real data and offering a robust solution for simulating nanopore sequencing signals with the latest flow cell generation. AVAILABILITY AND IMPLEMENTATION: seq2squiggle is freely available on GitHub at: github.com/ZKI-PH-ImageAnalysis/seq2squiggle.

Indexed as

NanoporesNanopore SequencingSequence Analysis, DNAAlgorithmsComputer SimulationSoftware

Identifiers

PMID39710838
PMCPMC11729726

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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.