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Heterogeneity Analysis and Diagnosis of Complex Diseases Based on Deep Learning Method

机译:基于深度学习方法的复杂疾病异质性分析与诊断

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Understanding genetic mechanism of complex diseases is a serious challenge. Existing methods often neglect the heterogeneity phenomenon of complex diseases, resulting in lack of power or low reproducibility. Addressing heterogeneity when detecting epistatic single nucleotide polymorphisms (SNPs) can enhance the power of association studies and improve prediction performance of complex diseases diagnosis. In this study, we propose a three-stage framework including epistasis detection, clustering and prediction to address both epistasis and heterogeneity of complex diseases based on deep learning method. The epistasis detection stage applies a multi-objective optimization method to find several candidate sets of epistatic SNPs which contribute to different subtypes of complex diseases. Then, a K-means clustering algorithm is used to define subtypes of the case group. Finally, a deep learning model has been trained for disease prediction based on graphics processing unit (GPU). Experimental results on pure and heterogeneous datasets show that our method has potential practicality and can serve as a possible alternative to other methods. Therefore, when epistasis and heterogeneity exist at the same time, our method is especially suitable for diagnosis of complex diseases.
机译:了解复杂疾病的遗传机制是一个严峻的挑战。现有方法常常忽略了复杂疾病的异质性现象,导致缺乏功效或可重复性低。检测上位性单核苷酸多态性(SNP)时解决异质性可以增强关联研究的能力,并改善复杂疾病诊断的预测性能。在这项研究中,我们提出了一个包括上皮检测,聚类和预测的三个阶段的框架,以解决基于深度学习方法的复杂疾病的上皮和异质性。上位性检测阶段应用多目标优化方法来找到几种候选上位性SNP,这些上位性SNP有助于复杂疾病的不同亚型。然后,使用K均值聚类算法来定义案例组的子类型。最终,已经针对基于图形处理单元(GPU)的疾病预测训练了深度学习模型。在纯数据集和异构数据集上的实验结果表明,我们的方法具有潜在的实用性,可以作为其他方法的替代方法。因此,当上皮性和异质性同时存在时,我们的方法特别适合于复杂疾病的诊断。

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