CoraL: interpretable contrastive meta-learning for the prediction of cancer-associated ncRNA-encoded small peptides

Author:

Li Zhongshen12,Jin Junru12,He Wenjia34,Long Wentao12,Yu Haoqing12,Gao Xin34,Nakai Kenta56,Zou Quan7,Wei Leyi12

Affiliation:

1. Shandong University School of Software, , Jinan 250101 , China

2. Shandong University Joint SDU-NTU Centre for Artificial Intelligence Research (C-FAIR), , Jinan 250101 , China

3. King Abdullah University of Science and Technology (KAUST) Computer Science Program, Computer, Electrical and Mathematical Sciences and Engineering Division (CEMSE), , Thuwal , Saudi Arabia

4. King Abdullah University of Science and Technology (KAUST) Computational Bioscience Research Center (CBRC), , Thuwal , Saudi Arabia

5. The University of Tokyo Department of Computational Biology and Medical Sciences, , 5-1-5 Kashiwanoha, Kashiwa-shi, Chiba 277-8562 , Japan

6. The Institute of Medical Science, The University of Tokyo Human Genome Center, , 4-6-1 Shirokanedai Minato-ku, Tokyo 108-8639 , Japan

7. University of Electronic Science and Technology of China Institute of Fundamental and Frontier Sciences, , Chengdu, 610054 , China

Abstract

Abstract NcRNA-encoded small peptides (ncPEPs) have recently emerged as promising targets and biomarkers for cancer immunotherapy. Therefore, identifying cancer-associated ncPEPs is crucial for cancer research. In this work, we propose CoraL, a novel supervised contrastive meta-learning framework for predicting cancer-associated ncPEPs. Specifically, the proposed meta-learning strategy enables our model to learn meta-knowledge from different types of peptides and train a promising predictive model even with few labeled samples. The results show that our model is capable of making high-confidence predictions on unseen cancer biomarkers with only five samples, potentially accelerating the discovery of novel cancer biomarkers for immunotherapy. Moreover, our approach remarkably outperforms existing deep learning models on 15 cancer-associated ncPEPs datasets, demonstrating its effectiveness and robustness. Interestingly, our model exhibits outstanding performance when extended for the identification of short open reading frames derived from ncPEPs, demonstrating the strong prediction ability of CoraL at the transcriptome level. Importantly, our feature interpretation analysis discovers unique sequential patterns as the fingerprint for each cancer-associated ncPEPs, revealing the relationship among certain cancer biomarkers that are validated by relevant literature and motif comparison. Overall, we expect CoraL to be a useful tool to decipher the pathogenesis of cancer and provide valuable information for cancer research. The dataset and source code of our proposed method can be found at https://github.com/Johnsunnn/CoraL.

Funder

Natural Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Molecular Biology,Information Systems

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