TY - GEN
T1 - EELMCDA
T2 - 2024 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2024
AU - Wang, Zheng
AU - Wang, Lei
AU - You, Zhu Hong
AU - Wang, Lei
AU - Li, Yang
AU - Wang, Zhenyu
N1 - Publisher Copyright:
© 2024 IEEE.
PY - 2024
Y1 - 2024
N2 - Recent studies have indicated that circular RNAs (circRNAs) play a significant role in the diagnosis and treatment of disease. However, the prediction of associations between circRNAs and diseases using conventional biological methods is constrained by numerous factors. In this study, we proposed a novel computational model called EELMCDA that combines evolutionary ensemble learning (EEL) approach and matrix feature decomposition method to predict potential circRNA-disease associations. The model firstly integrates circRNA function information, disease semantic information, and circRNA and disease gaussian interaction profile kernel (GIPK) information into an integrated matrix and constructed the corresponding feature matrix, then uses the matrix feature decomposition algorithm to obtain its important feature, and finally adopted evolutionary ensemble learning module to predict circRNA-disease associations. The average accuracy of the EELMCDA model by 5-fold cross-validation on CircR2Disease, CircAtlasv2.0, Circ2Disease, and CircRNADisease datasets were 92.40%, 92.90%, 88.91%, and 90.74%, respectively. Moreover, in case studies, the 21 of the top 30 circRNA-disease pairs with the highest EELMCDA scores were validated in recent literatures. These results further demonstrate the effectiveness of EELMCDA in predicting circRNA-disease associations.
AB - Recent studies have indicated that circular RNAs (circRNAs) play a significant role in the diagnosis and treatment of disease. However, the prediction of associations between circRNAs and diseases using conventional biological methods is constrained by numerous factors. In this study, we proposed a novel computational model called EELMCDA that combines evolutionary ensemble learning (EEL) approach and matrix feature decomposition method to predict potential circRNA-disease associations. The model firstly integrates circRNA function information, disease semantic information, and circRNA and disease gaussian interaction profile kernel (GIPK) information into an integrated matrix and constructed the corresponding feature matrix, then uses the matrix feature decomposition algorithm to obtain its important feature, and finally adopted evolutionary ensemble learning module to predict circRNA-disease associations. The average accuracy of the EELMCDA model by 5-fold cross-validation on CircR2Disease, CircAtlasv2.0, Circ2Disease, and CircRNADisease datasets were 92.40%, 92.90%, 88.91%, and 90.74%, respectively. Moreover, in case studies, the 21 of the top 30 circRNA-disease pairs with the highest EELMCDA scores were validated in recent literatures. These results further demonstrate the effectiveness of EELMCDA in predicting circRNA-disease associations.
KW - circRNA-disease associations
KW - circRNAs
KW - evolutionary ensemble learning
KW - matrix feature decomposition
UR - http://www.scopus.com/inward/record.url?scp=85217277932&partnerID=8YFLogxK
U2 - 10.1109/BIBM62325.2024.10822623
DO - 10.1109/BIBM62325.2024.10822623
M3 - 会议稿件
AN - SCOPUS:85217277932
T3 - Proceedings - 2024 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2024
SP - 1199
EP - 1206
BT - Proceedings - 2024 IEEE International Conference on Bioinformatics and Biomedicine, BIBM 2024
A2 - Cannataro, Mario
A2 - Zheng, Huiru
A2 - Gao, Lin
A2 - Cheng, Jianlin
A2 - de Miranda, Joao Luis
A2 - Zumpano, Ester
A2 - Hu, Xiaohua
A2 - Cho, Young-Rae
A2 - Park, Taesung
PB - Institute of Electrical and Electronics Engineers Inc.
Y2 - 3 December 2024 through 6 December 2024
ER -