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Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes

BACKGROUND: Orthology characterizes genes of different organisms that arose from a single ancestral gene via speciation, in contrast to paralogy, which is assigned to genes that arose via gene duplication. An accurate orthology assignment is a crucial step for comparative genomic studies. Orthologou...

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Autores principales: Petersen, Malte, Meusemann, Karen, Donath, Alexander, Dowling, Daniel, Liu, Shanlin, Peters, Ralph S., Podsiadlowski, Lars, Vasilikopoulos, Alexandros, Zhou, Xin, Misof, Bernhard, Niehuis, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312442/
https://www.ncbi.nlm.nih.gov/pubmed/28209129
http://dx.doi.org/10.1186/s12859-017-1529-8
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author Petersen, Malte
Meusemann, Karen
Donath, Alexander
Dowling, Daniel
Liu, Shanlin
Peters, Ralph S.
Podsiadlowski, Lars
Vasilikopoulos, Alexandros
Zhou, Xin
Misof, Bernhard
Niehuis, Oliver
author_facet Petersen, Malte
Meusemann, Karen
Donath, Alexander
Dowling, Daniel
Liu, Shanlin
Peters, Ralph S.
Podsiadlowski, Lars
Vasilikopoulos, Alexandros
Zhou, Xin
Misof, Bernhard
Niehuis, Oliver
author_sort Petersen, Malte
collection PubMed
description BACKGROUND: Orthology characterizes genes of different organisms that arose from a single ancestral gene via speciation, in contrast to paralogy, which is assigned to genes that arose via gene duplication. An accurate orthology assignment is a crucial step for comparative genomic studies. Orthologous genes in two organisms can be identified by applying a so-called reciprocal search strategy, given that complete information of the organisms’ gene repertoire is available. In many investigations, however, only a fraction of the gene content of the organisms under study is examined (e.g., RNA sequencing). Here, identification of orthologous nucleotide or amino acid sequences can be achieved using a graph-based approach that maps nucleotide sequences to genes of known orthology. Existing implementations of this approach, however, suffer from algorithmic issues that may cause problems in downstream analyses. RESULTS: We present a new software pipeline, Orthograph, that addresses and solves the above problems and implements useful features for a wide range of comparative genomic and transcriptomic analyses. Orthograph applies a best reciprocal hit search strategy using profile hidden Markov models and maps nucleotide sequences to the globally best matching cluster of orthologous genes, thus enabling researchers to conveniently and reliably delineate orthologs and paralogs from transcriptomic and genomic sequence data. We demonstrate the performance of our approach on de novo-sequenced and assembled transcript libraries of 24 species of apoid wasps (Hymenoptera: Aculeata) as well as on published genomic datasets. CONCLUSION: With Orthograph, we implemented a best reciprocal hit approach to reference-based orthology prediction for coding nucleotide sequences such as RNAseq data. Orthograph is flexible, easy to use, open source and freely available at https://mptrsen.github.io/Orthograph. Additionally, we release 24 de novo-sequenced and assembled transcript libraries of apoid wasp species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1529-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-53124422017-02-24 Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes Petersen, Malte Meusemann, Karen Donath, Alexander Dowling, Daniel Liu, Shanlin Peters, Ralph S. Podsiadlowski, Lars Vasilikopoulos, Alexandros Zhou, Xin Misof, Bernhard Niehuis, Oliver BMC Bioinformatics Software BACKGROUND: Orthology characterizes genes of different organisms that arose from a single ancestral gene via speciation, in contrast to paralogy, which is assigned to genes that arose via gene duplication. An accurate orthology assignment is a crucial step for comparative genomic studies. Orthologous genes in two organisms can be identified by applying a so-called reciprocal search strategy, given that complete information of the organisms’ gene repertoire is available. In many investigations, however, only a fraction of the gene content of the organisms under study is examined (e.g., RNA sequencing). Here, identification of orthologous nucleotide or amino acid sequences can be achieved using a graph-based approach that maps nucleotide sequences to genes of known orthology. Existing implementations of this approach, however, suffer from algorithmic issues that may cause problems in downstream analyses. RESULTS: We present a new software pipeline, Orthograph, that addresses and solves the above problems and implements useful features for a wide range of comparative genomic and transcriptomic analyses. Orthograph applies a best reciprocal hit search strategy using profile hidden Markov models and maps nucleotide sequences to the globally best matching cluster of orthologous genes, thus enabling researchers to conveniently and reliably delineate orthologs and paralogs from transcriptomic and genomic sequence data. We demonstrate the performance of our approach on de novo-sequenced and assembled transcript libraries of 24 species of apoid wasps (Hymenoptera: Aculeata) as well as on published genomic datasets. CONCLUSION: With Orthograph, we implemented a best reciprocal hit approach to reference-based orthology prediction for coding nucleotide sequences such as RNAseq data. Orthograph is flexible, easy to use, open source and freely available at https://mptrsen.github.io/Orthograph. Additionally, we release 24 de novo-sequenced and assembled transcript libraries of apoid wasp species. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12859-017-1529-8) contains supplementary material, which is available to authorized users. BioMed Central 2017-02-16 /pmc/articles/PMC5312442/ /pubmed/28209129 http://dx.doi.org/10.1186/s12859-017-1529-8 Text en © The Author(s) 2017 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Software
Petersen, Malte
Meusemann, Karen
Donath, Alexander
Dowling, Daniel
Liu, Shanlin
Peters, Ralph S.
Podsiadlowski, Lars
Vasilikopoulos, Alexandros
Zhou, Xin
Misof, Bernhard
Niehuis, Oliver
Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title_full Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title_fullStr Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title_full_unstemmed Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title_short Orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
title_sort orthograph: a versatile tool for mapping coding nucleotide sequences to clusters of orthologous genes
topic Software
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5312442/
https://www.ncbi.nlm.nih.gov/pubmed/28209129
http://dx.doi.org/10.1186/s12859-017-1529-8
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