TY  - JOUR
A1  - Diensthuber, Gregor
A1  - Pryszcz, Leszek P.
A1  - Llovera, Laia
A1  - Lucas, Morghan C.
A1  - Delgado-Tejedor, Anna
A1  - Cruciani, Sonia
A1  - Roignant, Jean-Yves
A1  - Begik, Oguzhan
A1  - Novoa, Eva Maria
T1  - Enhanced detection of RNA modifications and read mapping with high-accuracy nanopore RNA basecalling models
Y1  - 2024/11/01 
JF  - Genome Research 
JO  - Genome Research 
SP  - 1865 
EP  - 1877 
DO  - 10.1101/gr.278849.123 
VL  - 34 
IS  - 11 
UR  - http://genome.cshlp.org/content/34/11/1865.abstract 
N2  - In recent years, nanopore direct RNA sequencing (DRS) became a valuable tool for studying the epitranscriptome, owing to its ability to detect multiple modifications within the same full-length native RNA molecules. Although RNA modifications can be identified in the form of systematic basecalling “errors” in DRS data sets, N6-methyladenosine (m6A) modifications produce relatively low “errors” compared with other RNA modifications, limiting the applicability of this approach to m6A sites that are modified at high stoichiometries. Here, we demonstrate that the use of alternative RNA basecalling models, trained with fully unmodified sequences, increases the “error” signal of m6A, leading to enhanced detection and improved sensitivity even at low stoichiometries. Moreover, we find that high-accuracy alternative RNA basecalling models can show up to 97% median basecalling accuracy, outperforming currently available RNA basecalling models, which show 91% median basecalling accuracy. Notably, the use of high-accuracy basecalling models is accompanied by a significant increase in the number of mapped reads—especially in shorter RNA fractions—and increased basecalling error signatures at pseudouridine (Ψ)- and N1-methylpseudouridine (m1Ψ)-modified sites. Overall, our work demonstrates that alternative RNA basecalling models can be used to improve the detection of RNA modifications, read mappability, and basecalling accuracy in nanopore DRS data sets. 
ER  -