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MAP2: multiple alignment of syntenic genomic sequences

We describe a multiple alignment program named MAP2 based on a generalized pairwise global alignment algorithm for handling long, different intergenic and intragenic regions in genomic sequences. The MAP2 program produces an ordered list of local multiple alignments of similar regions among sequence...

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Detalles Bibliográficos
Autores principales: Ye, Liang, Huang, Xiaoqiu
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546147/
https://www.ncbi.nlm.nih.gov/pubmed/15640451
http://dx.doi.org/10.1093/nar/gki159
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author Ye, Liang
Huang, Xiaoqiu
author_facet Ye, Liang
Huang, Xiaoqiu
author_sort Ye, Liang
collection PubMed
description We describe a multiple alignment program named MAP2 based on a generalized pairwise global alignment algorithm for handling long, different intergenic and intragenic regions in genomic sequences. The MAP2 program produces an ordered list of local multiple alignments of similar regions among sequences, where different regions between local alignments are indicated by reporting only similar regions. We propose two similarity measures for the evaluation of the performance of MAP2 and existing multiple alignment programs. Experimental results produced by MAP2 on four real sets of orthologous genomic sequences show that MAP2 rarely missed a block of transitively similar regions and that MAP2 never produced a block of regions that are not transitively similar. Experimental results by MAP2 on six simulated data sets show that MAP2 found the boundaries between similar and different regions precisely. This feature is useful for finding conserved functional elements in genomic sequences. The MAP2 program is freely available in source code form at for academic use.
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spelling pubmed-5461472005-02-07 MAP2: multiple alignment of syntenic genomic sequences Ye, Liang Huang, Xiaoqiu Nucleic Acids Res Article We describe a multiple alignment program named MAP2 based on a generalized pairwise global alignment algorithm for handling long, different intergenic and intragenic regions in genomic sequences. The MAP2 program produces an ordered list of local multiple alignments of similar regions among sequences, where different regions between local alignments are indicated by reporting only similar regions. We propose two similarity measures for the evaluation of the performance of MAP2 and existing multiple alignment programs. Experimental results produced by MAP2 on four real sets of orthologous genomic sequences show that MAP2 rarely missed a block of transitively similar regions and that MAP2 never produced a block of regions that are not transitively similar. Experimental results by MAP2 on six simulated data sets show that MAP2 found the boundaries between similar and different regions precisely. This feature is useful for finding conserved functional elements in genomic sequences. The MAP2 program is freely available in source code form at for academic use. Oxford University Press 2005 2005-01-07 /pmc/articles/PMC546147/ /pubmed/15640451 http://dx.doi.org/10.1093/nar/gki159 Text en © 2005, the authors Nucleic Acids Research, Vol. 33 No. 1 © Oxford University Press 2005; all rights reserved
spellingShingle Article
Ye, Liang
Huang, Xiaoqiu
MAP2: multiple alignment of syntenic genomic sequences
title MAP2: multiple alignment of syntenic genomic sequences
title_full MAP2: multiple alignment of syntenic genomic sequences
title_fullStr MAP2: multiple alignment of syntenic genomic sequences
title_full_unstemmed MAP2: multiple alignment of syntenic genomic sequences
title_short MAP2: multiple alignment of syntenic genomic sequences
title_sort map2: multiple alignment of syntenic genomic sequences
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC546147/
https://www.ncbi.nlm.nih.gov/pubmed/15640451
http://dx.doi.org/10.1093/nar/gki159
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