基于密集多项式维数预测器的急性髓系白血病预测学习模型

K. Venkatesh, S. Pasupathy, S. Raja
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引用次数: 0

摘要

微阵列数据的分析非常复杂,是近年来研究的热点。基于机器学习的急性髓系白血病(Acute Myeloid Leukemia, AML)预测在自动诊断疾病严重程度和任何故障的预测中显示出巨大的影响。设计相应的分类器来处理大数据量大数据量的分类器是非常重要的。深度学习是一种更新的机器学习方法,可以缓解这些问题。由于存在大量的隐藏层,使得海量数据易于处理。所提出的分类方法用于理解所提出的基于密集多项式维数的预测模型()的训练。隐藏的神经元数量足够大,因此所提出的方法可以用来预测AML。AML和ALL样本在深度网络模型中使用五层进行分类。数据被划分为20%的数据和80%的网络测试和训练数据。与其他分类器相比,所提出的分类器的满意结果更高,更令人满意。在Kaggle、Gene expression和Bio GPS三个数据集上进行验证,使用Kaggle时,准确率为96%,精密度为94%,召回率为96%,F1-score为96%,AUROC为98%;使用Gene expression时,准确率达到95.50%,精密度为94%,召回率为95%,f1评分为96%,AUROC为96%;使用Bio GPS时,准确率达到98%,精密度为94.5%,召回率为98.5%,f1评分为96%,AUROC为94%。基于此分析,证明了该模型与所提出的模型很好地吻合,并建立了更好的权衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A Learning Model for Acute Myeloid Leukemia Prediction Using Dense Polynomial Dimensionality-Based Predictor
Analysis of microarray data is extremely complex and considered as a hot topic in recent research. Acute Myeloid Leukemia (AML) prediction based on machine learning shows huge impact on prediction which automatically diagnoses the disease severity and any malfunctions. It is important to design the relevant classifier that processes the large data volume with large data size. Deep learning is an updated machine learning approach for mitigating these issues. It is easy to handle the huge volume of data because of the large number of hidden layers. The proposed classification methodology is used for understanding the training of the proposed Dense Polynomial Dimensionality based Predictor Model (). The hidden neuron numbers are large in a sufficient way where the proposed is elaborated to predict AML. AML and ALL samples are classified using five layers in the deep network model. The data is partitioned as 20% data and 80% data testing and training in the network. Compared with other classifiers, the satisfying outcome from the proposed is higher and fulfilling. The validation is done in three datasets: Kaggle, Gene expression and Bio GPS and it gives 96% accuracy, 94% precision, 96% recall, 96% F1-score, and 98% AUROC while executing with Kaggle; then, 95.50% accuracy, 94% precision, 95% recall, 96% F1-score, and 96% AUROC is achieved while executing with Gene expression and finally 98% accuracy, 94.5% precision, 98.5% recall, 96% F1-score, and 94% AUROC is achieved while executing with Bio GPS. Based on this analysis, it is proven that the model works well with the proposed and establishes a better trade-off.
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