基于深度学习的复杂疾病检测的高性能计算

Sahar I. Ghanem, A. A. Ghoneim, Nagia M. Ghanem, M. Ismail
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引用次数: 0

摘要

全基因组关联研究(GWAS)与复杂疾病的研究是当前研究的热点。上位分析了单核苷酸多态性(snp)相互作用及其对复杂疾病的影响。然而,需要对大量的snp相互作用进行测试,以对抗这种计算成本很高的疾病。在本文中,高性能计算(HPC)被应用在超级计算机上,以减少处理时间。并行深度学习(PDL)在不同的数据集上进行了应用和测试。12种不同模型的模拟数据集和真实的WTCCC类风湿性关节炎(RA)数据集正在进行测试。结果表明,该方法具有较高的准确性、特异性和真阳性率。此外,通过不同的仿真模型,他们显示了较低的错误发现率和功率的鲁棒性。当在真实RA数据集上进行测试时,由于并行深度学习架构,我们的模型显示出能够以高精度检测与其有希望的相关基因的双向相互作用snp的能力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High Performance Computing for Detecting Complex Diseases using Deep Learning
The study of the Genome-wide association study (GWAS) and the complex diseases is of high importance nowadays. The epistasis describes the analysis of the single nucleotide polymorphisms (SNPs) interactions and their effects on the complex diseases. However, enormous number of SNPs interactions should be tested against the disease that is highly computational expensive. In this paper, High Performance Computing (HPC) is being applied on a supercomputer to reduce the processing time. Parallel Deep Learning (PDL) is applied and tested using different datasets. Simulated datasets of 12 different models and the real WTCCC Rheumatoid arthritis (RA) dataset are being tested. Results show the high accuracy, specificity and true positive rate values. Moreover, they show low values of the false discovery rate and the robustness of power through the different simulated models. When tested on the real RA dataset, our model shows the ability to detect the 2-way interaction SNPs with their promising related genes with high accuracy due to the parallel deep learning architecture.
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