Uncalled4 improves nanopore DNA and RNA modification detection via fast and accurate signal alignment

Nanopore signal analysis enables detection of nucleotide modifications from native DNA and RNA sequencing, providing both accurate genetic or transcriptomic and epigenetic information without additional library preparation. At present, only a limited set of modifications can be directly basecalled (for example, 5-methylcytosine), while most others require exploratory methods that often begin with alignment of nanopore signal to a nucleotide reference. We present Uncalled4, a toolkit for nanopore signal alignment, analysis and visualization. Uncalled4 features an efficient banded signal alignment algorithm, BAM signal alignment file format, statistics for comparing signal alignment methods and a reproducible de novo training method for k-mer-based pore models, revealing potential errors in Oxford Nanopore Technologies' state-of-the-art DNA model. We apply Uncalled4 to RNA 6-methyladenine (m6A) detection in seven human cell lines, identifying 26% more modifications than Nanopolish using m6Anet, including in several genes where m6A has known implications in cancer. Uncalled4 is available open source at github.com/skovaka/uncalled4 .

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Publication Details

Journal
Nature Methods
Published
2025-03-28
DOI
https://doi.org/10.1038/s41592-025-02631-4
Citations
38
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
29.02

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article

Uncalled4 improves nanopore DNA and RNA modification detection via fast and accurate signal alignment

Roham Razaghi, Vikram S. Shivakumar, Michael C. Schatz, Paul W. Hook et al.
38 citations
Nature Methods
RNA modifications and cancer
29.02
article

Uncalled4 improves nanopore DNA and RNA modification detection via fast and accurate signal alignment

Roham Razaghi, Vikram S. Shivakumar, Michael C. Schatz, Paul W. Hook, Katharine M. Jenike, Luke B Morina, Winston Timp, Sam Kovaka
article en
38 citations

Abstract

Nanopore signal analysis enables detection of nucleotide modifications from native DNA and RNA sequencing, providing both accurate genetic or transcriptomic and epigenetic information without additional library preparation. At present, only a limited set of modifications can be directly basecalled (for example, 5-methylcytosine), while most others require exploratory methods that often begin with alignment of nanopore signal to a nucleotide reference. We present Uncalled4, a toolkit for nanopore signal alignment, analysis and visualization. Uncalled4 features an efficient banded signal alignment algorithm, BAM signal alignment file format, statistics for comparing signal alignment methods and a reproducible de novo training method for k-mer-based pore models, revealing potential errors in Oxford Nanopore Technologies' state-of-the-art DNA model. We apply Uncalled4 to RNA 6-methyladenine (m6A) detection in seven human cell lines, identifying 26% more modifications than Nanopolish using m6Anet, including in several genes where m6A has known implications in cancer. Uncalled4 is available open source at github.com/skovaka/uncalled4 .

Nature MethodsVol. 22(4)
Johns Hopkins University (US), Johns Hopkins Medicine (US)
National Science Foundation, Lustgarten Foundation, Baylor College of Medicine, Maryland Advanced Research Computing Center, National Institutes of Health, National Human Genome Research Institute, National Cancer Institute
Openalex Percentile: Top 0%
RNA modifications and cancer
29.02
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