Jul 2026· Annual International Computer Software and Applications Conference· pp. 3022-3027· 0 citations· 13 references
Abstract
Small non-coding RNAs (ncRNAs) are functionally diverse RNA molecules involved in various regulatory and cellular processes. Accurate family classification of ncRNAs is important for large-scale functional annotation. However, many existing computational approaches rely heavily on predicted secondary structural information, which may not always be available. In this work, we propose a purely sequence-based deep learning framework for small ncRNA family classification without using explicit secondary structure features. Our approach combines one-hot encoded sequences, sequence-level motifs, normalized length, GC content, and biologically motivated handcrafted descriptors within a DenseNet-inspired convolutional neural network architecture. The proposed model was evaluated on the benchmark nRC dataset containing 13 ncRNA families using 10fold cross-validation and an independent test set. Our method achieved an MCC of 0.951 and an F1-score of 0.954, outperforming existing sequence-based as well as several structure-aware methods. The model also demonstrated improved performance for challenging classes such as miRNA, CD-box, HACA-box, and riboswitches. In addition, we evaluated the generalization capability of our framework on the recently introduced NCY dataset, where it maintained strong and consistent classification performance. These results show that enriched sequence-derived representations can effectively capture discriminative functional signals for ncRNA family classification without relying on secondary structure prediction. The source code is available at https://github.com/sharma-nandita/small_RNA_classification.
Identifying transcription factor binding sites (TFBSs) is fundamental to understanding complex gene regulatory mechanisms and the functions of non-coding regions. Although existing methods have achieved substantial strides, capturing both local structural features and long-range spatial dependencies within DNA sequence...
Jingjue Wei, Jie Feng· Match-communications in Math...· 0 citations
VAERNAGen, a novel variational autoencoder-based framework for de novo generation of RNA family sequences, outperformed the current state-of-the-art grammar-based method and is established as a state-of-the-art method for de novo generation of RNA family sequences.
Guohua Huang, Yu-Yan Li, Changdong Yu et al.· International Journal of Bio...· 0 citations
A concatenated deep neural network that incorporates both peptide and nucleotide embedding from masked language modeling (MLM), being able to discover complex associations between sequence information and lncRNA classification.
Zongrui Dai, Feiyang Deng, Hsiao H. Sung· bioRxiv· 4 citations
This study evaluates four encoding schemes—one-hot, k-mer (substring-based encoding), embeddings, and Position-Specific Scoring Matrix (PSSM) using Convolutional Neural Networks (CNNs) and Long Short-Term Memories (LSTMs) and shows that k-mer encoding achieved the highest accuracy.
T. Kurniawan, Deshinta Arova Dewi, Randy Joy Magno Ventayen· Journal of Advances in Infor...· 0 citations
This version introduces a unified Random Forest model trained on an expanded set of proxy-neutral and proxy-deleterious variants drawn from human and non-human primate genomes, and substantially improves the computational workflow, increasing predictive power for genome-wide SV interpretation.
The novel combination of LZ complexity–based negative sample selection, CT feature representation, and GA-optimized CNN–LSTM architecture provides a robust and biologically informed framework for PPI prediction.