Dissertation/ Thesis

Evolutionary Algorithms for Multiple Sequence Alignments

Λεπτομέρειες βιβλιογραφικής εγγραφής
Τίτλος: Evolutionary Algorithms for Multiple Sequence Alignments
Συγγραφείς: Naznin, Farhana
Στοιχεία εκδότη: UNSW, Sydney
Έτος έκδοσης: 2011
Συλλογή: UNSW Sydney (The University of New South Wales): UNSWorks
Θεματικοί όροι: Amino Acid Sequences, Deoxyribonucleic Acid, Ribonucleic Acid, Dynamic Algorithm / Programming, Pairwise Sequence Alignment, Guide Tree / Progressive Alignment Approach, Multiple Sequence Alignment, Iterative Approach, Genetic Algorithm
Περιγραφή: Multiple sequence alignment (MSA) is a valuable technique for studying molecular evolution, analysing sequence structure, and drug design. To date, in the literature, many algorithms for solving the MSA problems, based on progressive, iterative and stochastic approaches, have been proposed. As their performances vary depending on the characteristics of the test problems, there is a need for an effective algorithm that consistently performs better over a range of problems. Therefore, the objective of this thesis was to develop a new algorithm for solving MSA problems more effectively. However, our systematic analyses of the existing approaches encouraged us to propose not only a new algorithm but also the sequential development of increasingly effective algorithms. Firstly, this thesis presents a new iterative method, namely MSA-IT, which has two new mechanisms: the first generates guide trees with randomly selected sequences; and the second shuffles the sequences inside these trees, within an iterative process, to generate new and better guide trees. This method is simple and fast. Its performance was tested on standard benchmark problems and, compared with well-known algorithms, was convincing. However, as its solutions made clear that there was room for further improvement, we developed another algorithm based on a genetic algorithm with a progressive alignment approach, namely GAPAM. In GAPAM, the initial population is generated using the two mechanisms used in MSA-IT, and two new genetic search operators are implemented. To test its performance on benchmark datasets, the results from GAPAM were compared with those from MSA-IT as well as the well-known algorithms. The comparisons showed that GAPAM not only provides better solutions than MSA-IT and the other algorithms for most of the test problems, but also achieves an overall better performance. However, analyses of the results uncovered the fact that, for sequences of longer length, GAPAM was trapped in local optima. To overcome this local optima problem, ...
Τύπος εγγράφου: doctoral or postdoctoral thesis
Περιγραφή αρχείου: application/pdf
Γλώσσα: English
Relation: https://hdl.handle.net/1959.4/51535; https://doi.org/10.26190/unsworks/15176
DOI: 10.26190/unsworks/15176
Διαθεσιμότητα: https://hdl.handle.net/1959.4/51535
https://unsworks.unsw.edu.au/bitstreams/8e11d1c2-0ff5-4ff1-938a-d0b70ddb1436/download
https://doi.org/10.26190/unsworks/15176
Rights: open access ; https://purl.org/coar/access_right/c_abf2 ; CC BY-NC-ND 3.0 ; https://creativecommons.org/licenses/by-nc-nd/3.0/au/ ; free_to_read
Αριθμός Καταχώρησης: edsbas.246EB642
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  Data: Evolutionary Algorithms for Multiple Sequence Alignments
– Name: Author
  Label: Authors
  Group: Au
  Data: <searchLink fieldCode="AR" term="%22Naznin%2C+Farhana%22">Naznin, Farhana</searchLink>
– Name: Publisher
  Label: Publisher Information
  Group: PubInfo
  Data: UNSW, Sydney
– Name: DatePubCY
  Label: Publication Year
  Group: Date
  Data: 2011
– Name: Subset
  Label: Collection
  Group: HoldingsInfo
  Data: UNSW Sydney (The University of New South Wales): UNSWorks
– Name: Subject
  Label: Subject Terms
  Group: Su
  Data: <searchLink fieldCode="DE" term="%22Amino+Acid+Sequences%22">Amino Acid Sequences</searchLink><br /><searchLink fieldCode="DE" term="%22Deoxyribonucleic+Acid%22">Deoxyribonucleic Acid</searchLink><br /><searchLink fieldCode="DE" term="%22Ribonucleic+Acid%22">Ribonucleic Acid</searchLink><br /><searchLink fieldCode="DE" term="%22Dynamic+Algorithm+%2F+Programming%22">Dynamic Algorithm / Programming</searchLink><br /><searchLink fieldCode="DE" term="%22Pairwise+Sequence+Alignment%22">Pairwise Sequence Alignment</searchLink><br /><searchLink fieldCode="DE" term="%22Guide+Tree+%2F+Progressive+Alignment+Approach%22">Guide Tree / Progressive Alignment Approach</searchLink><br /><searchLink fieldCode="DE" term="%22Multiple+Sequence+Alignment%22">Multiple Sequence Alignment</searchLink><br /><searchLink fieldCode="DE" term="%22Iterative+Approach%22">Iterative Approach</searchLink><br /><searchLink fieldCode="DE" term="%22Genetic+Algorithm%22">Genetic Algorithm</searchLink>
– Name: Abstract
  Label: Description
  Group: Ab
  Data: Multiple sequence alignment (MSA) is a valuable technique for studying molecular evolution, analysing sequence structure, and drug design. To date, in the literature, many algorithms for solving the MSA problems, based on progressive, iterative and stochastic approaches, have been proposed. As their performances vary depending on the characteristics of the test problems, there is a need for an effective algorithm that consistently performs better over a range of problems. Therefore, the objective of this thesis was to develop a new algorithm for solving MSA problems more effectively. However, our systematic analyses of the existing approaches encouraged us to propose not only a new algorithm but also the sequential development of increasingly effective algorithms. Firstly, this thesis presents a new iterative method, namely MSA-IT, which has two new mechanisms: the first generates guide trees with randomly selected sequences; and the second shuffles the sequences inside these trees, within an iterative process, to generate new and better guide trees. This method is simple and fast. Its performance was tested on standard benchmark problems and, compared with well-known algorithms, was convincing. However, as its solutions made clear that there was room for further improvement, we developed another algorithm based on a genetic algorithm with a progressive alignment approach, namely GAPAM. In GAPAM, the initial population is generated using the two mechanisms used in MSA-IT, and two new genetic search operators are implemented. To test its performance on benchmark datasets, the results from GAPAM were compared with those from MSA-IT as well as the well-known algorithms. The comparisons showed that GAPAM not only provides better solutions than MSA-IT and the other algorithms for most of the test problems, but also achieves an overall better performance. However, analyses of the results uncovered the fact that, for sequences of longer length, GAPAM was trapped in local optima. To overcome this local optima problem, ...
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  Data: 10.26190/unsworks/15176
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  Data: https://hdl.handle.net/1959.4/51535<br />https://unsworks.unsw.edu.au/bitstreams/8e11d1c2-0ff5-4ff1-938a-d0b70ddb1436/download<br />https://doi.org/10.26190/unsworks/15176
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  Data: open access ; https://purl.org/coar/access_right/c_abf2 ; CC BY-NC-ND 3.0 ; https://creativecommons.org/licenses/by-nc-nd/3.0/au/ ; free_to_read
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        Value: 10.26190/unsworks/15176
    Languages:
      – Text: English
    Subjects:
      – SubjectFull: Amino Acid Sequences
        Type: general
      – SubjectFull: Deoxyribonucleic Acid
        Type: general
      – SubjectFull: Ribonucleic Acid
        Type: general
      – SubjectFull: Dynamic Algorithm / Programming
        Type: general
      – SubjectFull: Pairwise Sequence Alignment
        Type: general
      – SubjectFull: Guide Tree / Progressive Alignment Approach
        Type: general
      – SubjectFull: Multiple Sequence Alignment
        Type: general
      – SubjectFull: Iterative Approach
        Type: general
      – SubjectFull: Genetic Algorithm
        Type: general
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      – TitleFull: Evolutionary Algorithms for Multiple Sequence Alignments
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              Y: 2011
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