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Manipulating multiple sequence alignments via MaM and WebMaM

MaM is a software tool that processes and manipulates multiple alignments of genomic sequence. MaM computes the exact location of common repeat elements, exons and unique regions within aligned genomics sequences using a variety of user identified programs, databases and/or tables. The program can e...

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Detalles Bibliográficos
Autores principales: Alkan, Can, Tüzün, Eray, Buard, Jerome, Lethiec, Franck, Eichler, Evan E., Bailey, Jeffrey A., Sahinalp, S. Cenk
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2005
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160167/
https://www.ncbi.nlm.nih.gov/pubmed/15980474
http://dx.doi.org/10.1093/nar/gki406
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author Alkan, Can
Tüzün, Eray
Buard, Jerome
Lethiec, Franck
Eichler, Evan E.
Bailey, Jeffrey A.
Sahinalp, S. Cenk
author_facet Alkan, Can
Tüzün, Eray
Buard, Jerome
Lethiec, Franck
Eichler, Evan E.
Bailey, Jeffrey A.
Sahinalp, S. Cenk
author_sort Alkan, Can
collection PubMed
description MaM is a software tool that processes and manipulates multiple alignments of genomic sequence. MaM computes the exact location of common repeat elements, exons and unique regions within aligned genomics sequences using a variety of user identified programs, databases and/or tables. The program can extract subalignments, corresponding to these various regions of DNA to be analyzed independently or in conjunction with other elements of genomic DNA. Graphical displays further allow an assessment of sequence variation throughout these different regions of the aligned sequence, providing separate displays for their repeat, non-repeat and coding portions of genomic DNA. The program should facilitate the phylogenetic analysis and processing of different portions of genomic sequence as part of large-scale sequencing efforts. MaM source code is freely available for non-commercial use at ; and the web interface WebMaM is hosted at .
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spelling pubmed-11601672005-06-29 Manipulating multiple sequence alignments via MaM and WebMaM Alkan, Can Tüzün, Eray Buard, Jerome Lethiec, Franck Eichler, Evan E. Bailey, Jeffrey A. Sahinalp, S. Cenk Nucleic Acids Res Article MaM is a software tool that processes and manipulates multiple alignments of genomic sequence. MaM computes the exact location of common repeat elements, exons and unique regions within aligned genomics sequences using a variety of user identified programs, databases and/or tables. The program can extract subalignments, corresponding to these various regions of DNA to be analyzed independently or in conjunction with other elements of genomic DNA. Graphical displays further allow an assessment of sequence variation throughout these different regions of the aligned sequence, providing separate displays for their repeat, non-repeat and coding portions of genomic DNA. The program should facilitate the phylogenetic analysis and processing of different portions of genomic sequence as part of large-scale sequencing efforts. MaM source code is freely available for non-commercial use at ; and the web interface WebMaM is hosted at . Oxford University Press 2005-07-01 2005-06-27 /pmc/articles/PMC1160167/ /pubmed/15980474 http://dx.doi.org/10.1093/nar/gki406 Text en © The Author 2005. Published by Oxford University Press. All rights reserved
spellingShingle Article
Alkan, Can
Tüzün, Eray
Buard, Jerome
Lethiec, Franck
Eichler, Evan E.
Bailey, Jeffrey A.
Sahinalp, S. Cenk
Manipulating multiple sequence alignments via MaM and WebMaM
title Manipulating multiple sequence alignments via MaM and WebMaM
title_full Manipulating multiple sequence alignments via MaM and WebMaM
title_fullStr Manipulating multiple sequence alignments via MaM and WebMaM
title_full_unstemmed Manipulating multiple sequence alignments via MaM and WebMaM
title_short Manipulating multiple sequence alignments via MaM and WebMaM
title_sort manipulating multiple sequence alignments via mam and webmam
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1160167/
https://www.ncbi.nlm.nih.gov/pubmed/15980474
http://dx.doi.org/10.1093/nar/gki406
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