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Machine Learning Based Big Data Processing Framework for Cancer Diagnosis Using Hidden Markov Model and GM Clustering

机译:基于机器学习的大数据处理癌症诊断使用隐马尔可夫模型和GM集群

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摘要

The change in the DNA is a form of genetic variation in the human genome. In addition, the DNA copy number change is also linked with the progression of many emerging diseases. Array-based Comparative Genomic Hybridization (CGH) is considered as a major task when measuring the DNA copy number change across the genome. Moreover, DNA copy number change is an essential measure to diagnose the cancer disease. Next generation sequencing is an important method for studying the spread of infectious disease qualitatively and quantitatively. CGH is widely used in continuous monitoring of copy number of thousands of genes throughout the genome. In recent years, the size of the DNA sequence data is very large. Hence, there is a need to use a scalable machine learning approach to overcome the various issues in DNA copy number change detection. In this paper, we use a Bayesian hidden Markov model (HMM) with Gaussian Mixture (GM) Clustering approach to model the DNA copy number change across the genome. The proposed Bayesian HMM with GM Clustering approach is compared with various existing approaches such as Pruned Exact Linear Time method, binary segmentation method and segment neighborhood method. Experimental results demonstrate the effectiveness of our proposed change detection algorithm.
机译:DNA的变化是人类基因组的遗传变异形式。此外,DNA拷贝数变化也与许多新兴疾病的进展相关联。基于阵列的比较基因组杂交(CGH)被认为是在测量基因组上测量DNA拷贝数变化时的主要任务。此外,DNA拷贝数变化是诊断癌症疾病的重要措施。下一代测序是定性和定量地研究传染病传播的重要方法。 CGH广泛用于连续监测整个基因组的数千种基因的拷贝数。近年来,DNA序列数据的大小非常大。因此,需要使用可扩展的机器学习方法来克服DNA拷贝数变化检测中的各种问题。在本文中,我们使用具有高斯混合(GM)聚类方法的贝叶斯隐马尔可夫模型(HMM)来模拟基因组的DNA拷贝数变化。与GM集群方法的提议贝叶斯·嗯,与各种现有方法进行比较,例如修剪精确的线性时间方法,二进制分割方法和段邻域方法。实验结果表明了我们提出的改变检测算法的有效性。

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