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ArticleInterdisciplinary sciences, computational life sciences2025

MLWNNR: LncRNA-Disease Association Prediction with Multi-Kernel Learning-Driven Weighted Nuclear Norm Regularization.

Guo-Bo Xie, Hao-Jie Xu, Guo-Sheng Gu, Zhi-Yi Lin, Jun-Rui Yu, Rui-Bin Chen

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Article in Interdisciplinary sciences, computational life sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Guo-Bo XieSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China.
Hao-Jie XuSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China.
Guo-Sheng GuSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China. gsgu@gdut.edu.cn.ORCID http://orcid.org/0000-0002-0446-8255
Zhi-Yi LinSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China.
Jun-Rui YuSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China.
Rui-Bin ChenSchool of Computer Science, Guangdong University of Technology, Guangzhou, 510000, China.

Funding

the Discipline Co-construction Project of Guangdong Planning of Philosophy and Science GD18XJY07the Guangdong Philosophy and Social Sciences Planning Project GD21CJY24the National Natural Science Foundation of China 62002070
6 · The paper itself

Abstract

Emerging evidence highlights long non-coding RNAs (lncRNAs) as pivotal regulators demonstrating significant linkages with diverse human pathologies through expression dynamics and regulatory cascades. This research endeavors to establish an algorithm for forecasting the associations between lncRNAs and diseases based on multi-kernel learning-driven weighted nuclear norm regularization (MLWNNR). Specifically, our framework first uses a kernel learning algorithm centered on k-nearest neighbors to integrate multi-similarity kernels. Then, we construct a heterogeneous lncRNA-disease associations network utilizing similarity information and confirm lncRNA-disease associations. Finally, we adopt weighted nuclear norm regularization to complete the heterogeneous network to derive the final association prediction score. MLWNNR achieves impressive performance on three datasets and outperforms six representative models in the comparative experiments, which demonstrates its robustness and excellent generalization abilities. Furthermore, in case studies centered on three common human diseases, the majority of the hypothesized connections are corroborated by experimental literature. MLWNNR is a reliable approach for inferring lncRNA-disease associations, according to the experimental results.

Indexed as

Computational BiologyDiseaseMachine LearningRNA, Long NoncodingAlgorithmsHumansRNA, Long Noncodingdiseasek-nearest neighbor centered kernel learning algorithmlncRNAMulti-kernel learningWeighted nuclear norm regularization

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