Exploration of phylogenetic data using a global sequence analysis method

<p>Abstract</p> <p>Background</p> <p>Molecular phylogenetic methods are based on alignments of nucleic or peptidic sequences. The tremendous increase in molecular data permits phylogenetic analyses of very long sequences and of many species, but also requires methods to...

Full description

Bibliographic Details
Main Authors: Giron Alain, Edwards Scott, Dufraigne Christine, Chapus Charles, Fertil Bernard, Deschavanne Patrick
Format: Article
Language:English
Published: BMC 2005-11-01
Series:BMC Evolutionary Biology
Online Access:http://www.biomedcentral.com/1471-2148/5/63
_version_ 1818978896985456640
author Giron Alain
Edwards Scott
Dufraigne Christine
Chapus Charles
Fertil Bernard
Deschavanne Patrick
author_facet Giron Alain
Edwards Scott
Dufraigne Christine
Chapus Charles
Fertil Bernard
Deschavanne Patrick
author_sort Giron Alain
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Molecular phylogenetic methods are based on alignments of nucleic or peptidic sequences. The tremendous increase in molecular data permits phylogenetic analyses of very long sequences and of many species, but also requires methods to help manage large datasets.</p> <p>Results</p> <p>Here we explore the phylogenetic signal present in molecular data by genomic signatures, defined as the set of frequencies of short oligonucleotides present in DNA sequences. Although violating many of the standard assumptions of traditional phylogenetic analyses – in particular explicit statements of homology inherent in character matrices – the use of the signature does permit the analysis of very long sequences, even those that are unalignable, and is therefore most useful in cases where alignment is questionable. We compare the results obtained by traditional phylogenetic methods to those inferred by the signature method for two genes: RAG1, which is easily alignable, and 18S RNA, where alignments are often ambiguous for some regions. We also apply this method to a multigene data set of 33 genes for 9 bacteria and one archea species as well as to the whole genome of a set of 16 γ-proteobacteria. In addition to delivering phylogenetic results comparable to traditional methods, the comparison of signatures for the sequences involved in the bacterial example identified putative candidates for horizontal gene transfers.</p> <p>Conclusion</p> <p>The signature method is therefore a fast tool for exploring phylogenetic data, providing not only a pretreatment for discovering new sequence relationships, but also for identifying cases of sequence evolution that could confound traditional phylogenetic analysis.</p>
first_indexed 2024-12-20T16:50:56Z
format Article
id doaj.art-5b40312cc7214342a044bef7fb00a6b2
institution Directory Open Access Journal
issn 1471-2148
language English
last_indexed 2024-12-20T16:50:56Z
publishDate 2005-11-01
publisher BMC
record_format Article
series BMC Evolutionary Biology
spelling doaj.art-5b40312cc7214342a044bef7fb00a6b22022-12-21T19:32:49ZengBMCBMC Evolutionary Biology1471-21482005-11-01516310.1186/1471-2148-5-63Exploration of phylogenetic data using a global sequence analysis methodGiron AlainEdwards ScottDufraigne ChristineChapus CharlesFertil BernardDeschavanne Patrick<p>Abstract</p> <p>Background</p> <p>Molecular phylogenetic methods are based on alignments of nucleic or peptidic sequences. The tremendous increase in molecular data permits phylogenetic analyses of very long sequences and of many species, but also requires methods to help manage large datasets.</p> <p>Results</p> <p>Here we explore the phylogenetic signal present in molecular data by genomic signatures, defined as the set of frequencies of short oligonucleotides present in DNA sequences. Although violating many of the standard assumptions of traditional phylogenetic analyses – in particular explicit statements of homology inherent in character matrices – the use of the signature does permit the analysis of very long sequences, even those that are unalignable, and is therefore most useful in cases where alignment is questionable. We compare the results obtained by traditional phylogenetic methods to those inferred by the signature method for two genes: RAG1, which is easily alignable, and 18S RNA, where alignments are often ambiguous for some regions. We also apply this method to a multigene data set of 33 genes for 9 bacteria and one archea species as well as to the whole genome of a set of 16 γ-proteobacteria. In addition to delivering phylogenetic results comparable to traditional methods, the comparison of signatures for the sequences involved in the bacterial example identified putative candidates for horizontal gene transfers.</p> <p>Conclusion</p> <p>The signature method is therefore a fast tool for exploring phylogenetic data, providing not only a pretreatment for discovering new sequence relationships, but also for identifying cases of sequence evolution that could confound traditional phylogenetic analysis.</p>http://www.biomedcentral.com/1471-2148/5/63
spellingShingle Giron Alain
Edwards Scott
Dufraigne Christine
Chapus Charles
Fertil Bernard
Deschavanne Patrick
Exploration of phylogenetic data using a global sequence analysis method
BMC Evolutionary Biology
title Exploration of phylogenetic data using a global sequence analysis method
title_full Exploration of phylogenetic data using a global sequence analysis method
title_fullStr Exploration of phylogenetic data using a global sequence analysis method
title_full_unstemmed Exploration of phylogenetic data using a global sequence analysis method
title_short Exploration of phylogenetic data using a global sequence analysis method
title_sort exploration of phylogenetic data using a global sequence analysis method
url http://www.biomedcentral.com/1471-2148/5/63
work_keys_str_mv AT gironalain explorationofphylogeneticdatausingaglobalsequenceanalysismethod
AT edwardsscott explorationofphylogeneticdatausingaglobalsequenceanalysismethod
AT dufraignechristine explorationofphylogeneticdatausingaglobalsequenceanalysismethod
AT chapuscharles explorationofphylogeneticdatausingaglobalsequenceanalysismethod
AT fertilbernard explorationofphylogeneticdatausingaglobalsequenceanalysismethod
AT deschavannepatrick explorationofphylogeneticdatausingaglobalsequenceanalysismethod