Peng Jiajie, Bai Kun, Shang Xuequn, Wang Guohua, Xue Hansheng, Jin Shuilin, Cheng Liang, Wang Yadong, Chen Jin
School of Computer Science, Northwestern Polytechnical University, Xi'an, China.
School of Computer Science and Technology, Harbin Institute of Technology, Harbin, China.
BMC Genomics. 2017 Jan 25;18(Suppl 1):1043. doi: 10.1186/s12864-016-3263-4.
Identifying the genes associated to human diseases is crucial for disease diagnosis and drug design. Computational approaches, esp. the network-based approaches, have been recently developed to identify disease-related genes effectively from the existing biomedical networks. Meanwhile, the advance in biotechnology enables researchers to produce multi-omics data, enriching our understanding on human diseases, and revealing the complex relationships between genes and diseases. However, none of the existing computational approaches is able to integrate the huge amount of omics data into a weighted integrated network and utilize it to enhance disease related gene discovery.
We propose a new network-based disease gene prediction method called SLN-SRW (Simplified Laplacian Normalization-Supervised Random Walk) to generate and model the edge weights of a new biomedical network that integrates biomedical data from heterogeneous sources, thus far enhancing the disease related gene discovery.
The experiment results show that SLN-SRW significantly improves the performance of disease gene prediction on both the real and the synthetic data sets.
识别与人类疾病相关的基因对于疾病诊断和药物设计至关重要。计算方法,尤其是基于网络的方法,最近已被开发出来,以便从现有的生物医学网络中有效地识别疾病相关基因。同时,生物技术的进步使研究人员能够产生多组学数据,增进我们对人类疾病的理解,并揭示基因与疾病之间的复杂关系。然而,现有的计算方法都无法将大量的组学数据整合到一个加权综合网络中,并利用它来加强疾病相关基因的发现。
我们提出了一种新的基于网络的疾病基因预测方法,称为SLN-SRW(简化拉普拉斯归一化-监督随机游走),以生成和建模一个整合来自异质来源生物医学数据的新生物医学网络的边权重,从而加强疾病相关基因的发现。
实验结果表明,SLN-SRW在真实数据集和合成数据集上都显著提高了疾病基因预测的性能。