LKLPDA: A Low-Rank Fast Kernel Learning Approach for Predicting piRNA-Disease Associations.

IF 3.6 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Qingzhou Shi, Kai Zheng, Haoyuan Li, Bo Wang, Xiao Liang, Xinyu Li, Jianxin Wang
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引用次数: 0

Abstract

Piwi-interacting RNAs (piRNAs) are increasingly recognized as potential biomarkers for various diseases. Investig-ating the complex relationship between piRNAs and diseases through computational methods can reduce the costs and risks associated with biological experiments. Fast kernel learning (FKL) is a classical method for multi-source data fusion that is widely employed in association prediction research. However, biological networks are noisy due to the limitations of measurement technology and inherent natural variation, which can hamper the effectiveness of the network-based ideal kernel. The conventional FKL method does not address this issue. In this study, we propose a low-rank fast kernel learning (LRFKL) algorithm, which consists of low-rank representation (LRR) and the FKL algorithm. The LRFKL algorithm is designed to mitigate the effects of noise on the network-based ideal kernel. Using LRFKL, we propose a novel approach for predicting piRNA-disease associations called LKLPDA. Specifically, we first compute the similarity matrices for piRNAs and diseases. Then we use the LRFKL to fuse the similarity matrices for piRNAs and diseases separately. Finally, the LKLPDA employs AutoGluon-Tabular for predictive analysis. Computational results show that LKLPDA effectively predicts piRNA-disease associations with higher accuracy compared to previous methods. In addition, case studies confirm the reliability of the model in predicting piRNA-disease associations. Availability and implementation: The LKLPDA software and data are freely available at https://github.com/Shiqzz/LKLPDA-master.git.

LKLPDA:用于预测 piRNA 与疾病关联的低链快速核学习方法
越来越多的人认识到,πi-互作 RNA(piRNA)是各种疾病的潜在生物标志物。通过计算方法研究 piRNA 与疾病之间的复杂关系可以降低生物实验的成本和风险。快速核学习(FKL)是一种经典的多源数据融合方法,被广泛应用于关联预测研究。然而,由于测量技术的限制和固有的自然变异,生物网络存在噪声,这会影响基于网络的理想核的有效性。传统的 FKL 方法无法解决这一问题。在这项研究中,我们提出了一种低秩快速核学习(LRFKL)算法,它由低秩表示(LRR)和 FKL 算法组成。LRFKL 算法旨在减轻噪声对基于网络的理想内核的影响。利用 LRFKL,我们提出了一种预测 piRNA-疾病关联的新方法,称为 LKLPDA。具体来说,我们首先计算 piRNA 和疾病的相似性矩阵。然后,我们使用 LRFKL 分别融合 piRNA 和疾病的相似性矩阵。最后,LKLPDA 利用 AutoGluon-Tabular 进行预测分析。计算结果表明,与之前的方法相比,LKLPDA 能有效预测 piRNA 与疾病的关联,而且准确率更高。此外,案例研究也证实了该模型在预测 piRNA-疾病关联方面的可靠性。可用性和实施:LKLPDA 软件和数据可在 https://github.com/Shiqzz/LKLPDA-master.git 免费获取。
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来源期刊
CiteScore
7.50
自引率
6.70%
发文量
479
审稿时长
3 months
期刊介绍: IEEE/ACM Transactions on Computational Biology and Bioinformatics emphasizes the algorithmic, mathematical, statistical and computational methods that are central in bioinformatics and computational biology; the development and testing of effective computer programs in bioinformatics; the development of biological databases; and important biological results that are obtained from the use of these methods, programs and databases; the emerging field of Systems Biology, where many forms of data are used to create a computer-based model of a complex biological system
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