Recombination Hotspot/Coldspot Identification Combining Three Different Pseudocomponents via an Ensemble Learning Approach.

Recombination presents a nonuniform distribution across the genome. Genomic regions that present relatively higher frequencies of recombination are called hotspots while those with relatively lower frequencies of recombination are recombination coldspots. Therefore, the identification of hotspots/co...

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Publicado en:BioMed Research International Vol. 2016; pp. 1 - 8
Autores principales: Liu, Bingquan, Liu, Yumeng, Huang, Dong
Formato: equations & formulas pictorial research tables/charts Journal Article
Publicado: Wiley-Blackwell 8/25/2016
Acceso en línea:Ver este registro en EBSCOhost
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      dt: 8/25/2016
      vid: 2016
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      pub: Wiley-Blackwell
      place: Malden, Massachusetts
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        117669196
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        10.1155/2016/8527435
        117669196
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        atl: Recombination Hotspot/Coldspot Identification Combining Three Different Pseudocomponents via an Ensemble Learning Approach.
      aug:
        au:
          Liu, Bingquan
          Liu, Yumeng
          Huang, Dong
        affil: School of Computer Science and Technology, Harbin Institute of Technology, Harbin, Heilongjiang, China
      sug:
        subj:
          DNA, Recombinant
          Genomics
          Human
          Cell Physiology
          Models, Statistical
          Sequence Analysis
          Nucleotides
          Funding Source
      ab: Recombination presents a nonuniform distribution across the genome. Genomic regions that present relatively higher frequencies of recombination are called hotspots while those with relatively lower frequencies of recombination are recombination coldspots. Therefore, the identification of hotspots/coldspots could provide useful information for the study of the mechanism of recombination. In this study, a new computational predictor called SVM-EL was proposed to identify hotspots/coldspots across the yeast genome. It combined Support Vector Machines (SVMs) and Ensemble Learning (EL) based on three features including basic kmer (Kmer), dinucleotide-based auto-cross covariance (DACC), and pseudo dinucleotide composition (PseDNC). These features are able to incorporate the nucleic acid composition and their order information into the predictor. The proposed SVM-EL achieves an accuracy of 82.89% on a widely used benchmark dataset, which outperforms some related methods.
      pubtype: Academic Journal
      doctype:
        equations & formulas
        pictorial
        research
        tables/charts
        Journal Article
      ougenre: Article
    language: English
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