Nucleic Acids ResearchBioinformaticsPeer-reviewed journal article
WarpDemuX-tRNA: barcode multiplexing for nanopore tRNA sequencing
Wiep van der ToorniD, Isabel S. Naarmann‐de VriesiD, Wang Liu-WeiiD, Christoph DieterichiD, Max von KleistiD
Abstract
Transfer RNA (tRNA) plays an essential role in protein translation and tRNA modifications are important to their function. Recently, nanopore direct RNA sequencing (dRNA-seq) has shown promising results in the detection of complex tRNA modifications. However, its wider adoption in the tRNA field has been limited by a lack of (de)multiplexing solutions. Here, we present WarpDemuX-tRNA: an extension to the WarpDemuX method specifically optimized for multiplexed nanopore tRNA sequencing. Using consensus-based signal analysis using (soft) Dynamic Time Warping and barycenter averaging, our approach improves barcode feature generation and achieves more robust barcode identification. WarpDemuX-tRNA outperforms the original method and achieves 99% precision and 95% recovery for four barcodes, while reducing computational complexity and runtime to six minutes per one million reads. WarpDemuX-tRNA is an open-source and free-to-use solution to high-throughput nanopore tRNA sequencing, facilitating more accessible, cost-effective and high-throughput studies of tRNA modifications and their regulatory mechanisms.
- assay: long-read sequencing
- research focus: batch correction / integration
- approach: statistical model
- Citations
- 8
- FWCI
- 2.39
- Field percentile
- top 10%
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