BF-m7GPred: A Dual-Branch Feature Fusion Deep Learning Architecture for Identifying RNA N7-Methylguanosine Modification Sites

RNA N7-methylguanosine (m7G) is an important post-transcriptional epigenetic modification that participates in key biological processes, including RNA processing, stability maintenance, and translational regulation. Medical research has shown that m7G modification and its related regulatory factors are closely related to many neurological diseases and tumors. The accurate prediction of m7G sites is thus critical for understanding their biological functions in diseases. In this work, we propose BF-m7GPred, a dual-branch deep learning framework that integrates single-nucleotide-level embeddings and motif-level embeddings for m7G modification site prediction. Our proposed context-aware module tokenizes RNA sequences using byte-pair encoding and encodes sequences with the pretrained foundation biological model DNABERT2. In parallel, the proposed feature fusion module transforms sequences into multiple feature matrices using multiple traditional encoders. We introduce a feature selection strategy tailored to the encoding characteristics of the two branches. On a benchmark dataset collected from m7G-Hub v2.0, BF-m7GPred achieves superior performance on the independent test set against existing methods. Furthermore, its generalization capability is validated through comparative experiments on 10 diverse RNA modification datasets.