Author
Listed:
- Mahala Abhipsa
(Department of Computer Science & Engineering, C. V. Raman Global University, Bhubaneswar, Odisha, India)
- Ranjan Ashish
(Department of Computer Science & Engineering, C. V. Raman Global University, Bhubaneswar, Odisha, India)
- Priyadarshini Rojalina
(Department of Computer Science & Engineering, C. V. Raman Global University, Bhubaneswar, Odisha, India)
- Vikram Raj
(Department of Computer Science & Engineering, C. V. Raman Global University, Bhubaneswar, Odisha, India)
- Dansena Prabhat
(Department of Computer Science & Engineering, C. V. Raman Global University, Bhubaneswar, Odisha, India)
Abstract
The transformer model for sequence mining has brought a paradigmatic shift to many domains, including biological sequence mining. However, transformers suffer from quadratic complexity, i.e., O(l 2), where l is the sequence length, which affects the training and prediction time. Therefore, the work herein introduces a simple, generalized, and fast transformer architecture for improved protein function prediction. The proposed architecture uses a combination of CNN and global-average pooling to effectively shorten the protein sequences. The shortening process helps reduce the quadratic complexity of the transformer, resulting in the complexity of O((l/2)2). This architecture is utilized to develop PFP solution at the sub-sequence level. Furthermore, focal loss is employed to ensure balanced training for the hard-classified examples. The multi sub-sequence-based proposed solution utilizing an average-pooling layer (with stride = 2) produced improvements of +2.50 % (BP) and +3.00 % (MF) when compared to Global-ProtEnc Plus. The corresponding improvements when compared to the Lite-SeqCNN are: +4.50 % (BP) and +2.30 % (MF).
Suggested Citation
Mahala Abhipsa & Ranjan Ashish & Priyadarshini Rojalina & Vikram Raj & Dansena Prabhat, 2025.
"A fast (CNN + MCWS-transformer) based architecture for protein function prediction,"
Statistical Applications in Genetics and Molecular Biology, De Gruyter, vol. 24(1), pages 1-17.
Handle:
RePEc:bpj:sagmbi:v:24:y:2025:i:1:p:17:n:1001
DOI: 10.1515/sagmb-2024-0027
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