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


ABSTRACT: 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 [Formula: see text] and ?q (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.

SUBMITTER: Wang S 

PROVIDER: S-EPMC6375558 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

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

Wang Sai S   Shen Hai-Wei HW   Chai Hua H   Liang Yong Y  

PloS one 20190214 2


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  ...[more]

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