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Complex harmonic regularization with differential evolution in a memetic framework for biomarker selection

机译:在生物标记选择的模因框架中具有差分进化的复杂谐波正则化

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摘要

For studying cancer and genetic diseases, the issue of identifying high correlation genes from high-dimensional data is an important problem. It is a great challenge to select relevant biomarkers from gene expression data that contains some important correlation structures, and some of the genes can be divided into different groups with a common biological function, chromosomal location or regulation. In this paper, we propose a penalized accelerated failure time model CHR-DE using a non-convex regularization (local search) with differential evolution (global search) in a wrapper-embedded memetic framework. The complex harmonic regularization (CHR) can approximate to the combination p(12p<1) and ℓq (1 ≤ q < 2) for selecting biomarkers in group. And differential evolution (DE) is utilized to globally optimize the CHR’s hyperparameters, which make CHR-DE achieve strong capability of selecting groups of genes in high-dimensional biological data. We also developed an efficient path seeking algorithm to optimize this penalized model. The proposed method is evaluated on synthetic and three gene expression datasets: breast cancer, hepatocellular carcinoma and colorectal cancer. The experimental results demonstrate that CHR-DE is a more effective tool for feature selection and learning prediction.
机译:对于研究癌症和遗传疾病,从高维数据识别高相关基因的问题是一个重要的问题。从包含一些重要相关结构的基因表达数据中选择相关的生物标志物是一个巨大的挑战,并且某些基因可以分为具有共同生物学功能,染色体位置或调控的不同组。在本文中,我们提出了一种在包装器嵌入的模因框架中使用具有差分演化(全局搜索)的非凸正则化(局部搜索)的惩罚性加速失效时间模型CHR-DE。复谐波正则化(CHR)可以近似于 < msub> p < mn> 1 2 p / mo> 1 和ℓq(1≤q <2)来选择组中的生物标记。并且利用差异进化(DE)来全局优化CHR的超参数,这使CHR-DE拥有强大的选择高维生物学数据中基因组的能力。我们还开发了一种有效的路径搜索算法来优化此惩罚模型。该方法在合成和三个基因表达数据集上进行了评估:乳腺癌,肝细胞癌和结肠直肠癌。实验结果表明,CHR-DE是一种更有效的特征选择和学习预测工具。

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