Analysis of high-order SNP barcodes in mitochondrial D-loop for chronic dialysis susceptibility.

Objectives: Positively identifying disease-associated single nucleotide polymorphism (SNP) markers in genome-wide studies entails the complex association analysis of a huge number of SNPs. Such large numbers of SNP barcode (SNP/genotype combinations) continue to pose serious computational challenges...

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Publicado en:Journal of Biomedical Informatics Vol. 63; pp. 112 - 120
Autores principales: Yang, Cheng-Hong, Lin, Yu-Da, Chuang, Li-Yeh, Chang, Hsueh-Wei
Formato: research Journal Article
Publicado: Academic Press Inc. Oct2016
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Oct2016
      vid: 63
      pid: 735
      pub: Academic Press Inc.
      place: Burlington, Massachusetts
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        118967228
        118967228
        NLM27507088
        118967228
        10.1016/j.jbi.2016.08.009
        NLM27507088
        118967228
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        atl: Analysis of high-order SNP barcodes in mitochondrial D-loop for chronic dialysis susceptibility.
      aug:
        au:
          Yang, Cheng-Hong
          Lin, Yu-Da
          Chuang, Li-Yeh
          Chang, Hsueh-Wei
        affil: Department of Electronic Engineering, National Kaohsiung University of Applied Sciences, Kaohsiung, Taiwan
      sug:
        subj:
          Bar Coding
          Algorithms
          DNA
          Polymorphism, Genetic
          Hemodialysis Statistics and Numerical Data
          Genotype
          Human
      ab: Objectives: Positively identifying disease-associated single nucleotide polymorphism (SNP) markers in genome-wide studies entails the complex association analysis of a huge number of SNPs. Such large numbers of SNP barcode (SNP/genotype combinations) continue to pose serious computational challenges, especially for high-dimensional data.Methods: We propose a novel exploiting SNP barcode method based on differential evolution, termed IDE (improved differential evolution). IDE uses a "top combination strategy" to improve the ability of differential evolution to explore high-order SNP barcodes in high-dimensional data.Results: We simulate disease data and use real chronic dialysis data to test four global optimization algorithms. In 48 simulated disease models, we show that IDE outperforms existing global optimization algorithms in terms of exploring ability and power to detect the specific SNP/genotype combinations with a maximum difference between cases and controls. In real data, we show that IDE can be used to evaluate the relative effects of each individual SNP on disease susceptibility.Conclusion: IDE generated significant SNP barcode with less computational complexity than the other algorithms, making IDE ideally suited for analysis of high-order SNP barcodes.
      pubtype: Academic Journal
      doctype:
        research
        Journal Article
      ougenre: Article
    language: English
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