Freezing firefly algorithm for efficient planted (ℓ, d) motif search.

The detection of inimitable patterns (motif) occurring in a set of biological sequences could elevate new biological discoveries. Its application in recognition of transcription factors and their binding sites have demonstrated the necessity to attain knowledge of gene function, human diseases, and...

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Publicado en:Medical & Biological Engineering & Computing Vol. 60; no. 2; pp. 511 - 531
Autores principales: Theepalakshmi, P., Reddy, U. Srinivasulu
Formato: Journal Article
Publicado: Springer Nature Feb2022
Acceso en línea:Ver este registro en EBSCOhost
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      dt: Feb2022
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      pub: Springer Nature
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        atl: Freezing firefly algorithm for efficient planted (ℓ, d) motif search.
      aug:
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          Theepalakshmi, P.
          Reddy, U. Srinivasulu
        affil: Department of Computer Applications, National Institute of Technology, Tiruchirappalli, Tamilnadu, India
      sug:
        subj:
          Algorithms
          Magnetic Resonance Imaging
          Freezing
          Binding Sites
          Bioinformatics
          Coping Health Inventory for Parents
          Clinical Assessment Tools
          Scales
      ab: The detection of inimitable patterns (motif) occurring in a set of biological sequences could elevate new biological discoveries. Its application in recognition of transcription factors and their binding sites have demonstrated the necessity to attain knowledge of gene function, human diseases, and drug design. The literature identifies (ℓ, d) motif search as the widely studied problem in PMS (Planted Motif Search). This paper proposes an efficient optimization algorithm named "Freezing FireFly (FFF)" to solve (ℓ, d) motif search problem. The new strategy freezing such as local and global was added to increase the performance of the basic Firefly algorithm. It freezes the best possible out coming positions even in the lesser brighter one. The performance of the proposed algorithm is experienced on simulated and real datasets. The experimental results show that the proposed algorithm resolves the instance (50, 21) within 1.47 min in the simulated dataset. For real (such as ChIP-seq (Chromatin Immunoprecipitation)) and synthetic datasets, the proposed algorithm runs much faster in comparison to existing state-of-the-art optimization algorithms, including Samselect, TraverStringRef, PMS8, qPMS9, AlignACE, FMGA, and GSGA.
      pubtype: Academic Journal
      doctype: Journal Article
      ougenre: Article
    language: English
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