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Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment
BACKGROUND: Many Bioinformatics studies begin with a multiple sequence alignment as the foundation for their research. This is because multiple sequence alignment can be a useful technique for studying molecular evolution and analyzing sequence structure relationships. RESULTS: In this paper, we hav...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180391/ https://www.ncbi.nlm.nih.gov/pubmed/21867510 http://dx.doi.org/10.1186/1471-2105-12-353 |
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author | Naznin, Farhana Sarker, Ruhul Essam, Daryl |
author_facet | Naznin, Farhana Sarker, Ruhul Essam, Daryl |
author_sort | Naznin, Farhana |
collection | PubMed |
description | BACKGROUND: Many Bioinformatics studies begin with a multiple sequence alignment as the foundation for their research. This is because multiple sequence alignment can be a useful technique for studying molecular evolution and analyzing sequence structure relationships. RESULTS: In this paper, we have proposed a Vertical Decomposition with Genetic Algorithm (VDGA) for Multiple Sequence Alignment (MSA). In VDGA, we divide the sequences vertically into two or more subsequences, and then solve them individually using a guide tree approach. Finally, we combine all the subsequences to generate a new multiple sequence alignment. This technique is applied on the solutions of the initial generation and of each child generation within VDGA. We have used two mechanisms to generate an initial population in this research: the first mechanism is to generate guide trees with randomly selected sequences and the second is shuffling the sequences inside such trees. Two different genetic operators have been implemented with VDGA. To test the performance of our algorithm, we have compared it with existing well-known methods, namely PRRP, CLUSTALX, DIALIGN, HMMT, SB_PIMA, ML_PIMA, MULTALIGN, and PILEUP8, and also other methods, based on Genetic Algorithms (GA), such as SAGA, MSA-GA and RBT-GA, by solving a number of benchmark datasets from BAliBase 2.0. CONCLUSIONS: The experimental results showed that the VDGA with three vertical divisions was the most successful variant for most of the test cases in comparison to other divisions considered with VDGA. The experimental results also confirmed that VDGA outperformed the other methods considered in this research. |
format | Online Article Text |
id | pubmed-3180391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31803912011-09-27 Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment Naznin, Farhana Sarker, Ruhul Essam, Daryl BMC Bioinformatics Research Article BACKGROUND: Many Bioinformatics studies begin with a multiple sequence alignment as the foundation for their research. This is because multiple sequence alignment can be a useful technique for studying molecular evolution and analyzing sequence structure relationships. RESULTS: In this paper, we have proposed a Vertical Decomposition with Genetic Algorithm (VDGA) for Multiple Sequence Alignment (MSA). In VDGA, we divide the sequences vertically into two or more subsequences, and then solve them individually using a guide tree approach. Finally, we combine all the subsequences to generate a new multiple sequence alignment. This technique is applied on the solutions of the initial generation and of each child generation within VDGA. We have used two mechanisms to generate an initial population in this research: the first mechanism is to generate guide trees with randomly selected sequences and the second is shuffling the sequences inside such trees. Two different genetic operators have been implemented with VDGA. To test the performance of our algorithm, we have compared it with existing well-known methods, namely PRRP, CLUSTALX, DIALIGN, HMMT, SB_PIMA, ML_PIMA, MULTALIGN, and PILEUP8, and also other methods, based on Genetic Algorithms (GA), such as SAGA, MSA-GA and RBT-GA, by solving a number of benchmark datasets from BAliBase 2.0. CONCLUSIONS: The experimental results showed that the VDGA with three vertical divisions was the most successful variant for most of the test cases in comparison to other divisions considered with VDGA. The experimental results also confirmed that VDGA outperformed the other methods considered in this research. BioMed Central 2011-08-25 /pmc/articles/PMC3180391/ /pubmed/21867510 http://dx.doi.org/10.1186/1471-2105-12-353 Text en Copyright ©2011 Naznin et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Naznin, Farhana Sarker, Ruhul Essam, Daryl Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title | Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title_full | Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title_fullStr | Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title_full_unstemmed | Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title_short | Vertical decomposition with Genetic Algorithm for Multiple Sequence Alignment |
title_sort | vertical decomposition with genetic algorithm for multiple sequence alignment |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3180391/ https://www.ncbi.nlm.nih.gov/pubmed/21867510 http://dx.doi.org/10.1186/1471-2105-12-353 |
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