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Phylogenetic reconstruction from transpositions

BACKGROUND: Because of the advent of high-throughput sequencing and the consequent reduction in the cost of sequencing, many organisms have been completely sequenced and most of their genes identified. It thus has become possible to represent whole genomes as ordered lists of gene identifiers and to...

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Autores principales: Yue, Feng, Zhang, Meng, Tang, Jijun
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2559879/
https://www.ncbi.nlm.nih.gov/pubmed/18831780
http://dx.doi.org/10.1186/1471-2164-9-S2-S15
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author Yue, Feng
Zhang, Meng
Tang, Jijun
author_facet Yue, Feng
Zhang, Meng
Tang, Jijun
author_sort Yue, Feng
collection PubMed
description BACKGROUND: Because of the advent of high-throughput sequencing and the consequent reduction in the cost of sequencing, many organisms have been completely sequenced and most of their genes identified. It thus has become possible to represent whole genomes as ordered lists of gene identifiers and to study the rearrangement of these entities through computational means. As a result, genome rearrangement data has attracted increasing attentions from both biologists and computer scientists as a new type of data for phylogenetic analysis. The main events of genome rearrangements include inversions, transpositions and transversions. To date, GRAPPA and MGR are the most accurate methods for rearrangement phylogeny, both assuming inversion as the only event. However, due to the complexity of computing transposition distance, it is very difficult to analyze datasets when transpositions are dominant. RESULTS: We extend GRAPPA to handle transpositions. The new method is named GRAPPA-TP, with two major extensions: a heuristic method to estimate transposition distance, and a new transposition median solver for three genomes. Although GRAPPA-TP uses a greedy approach to compute the transposition distance, it is very accurate when genomes are relatively close. The new GRAPPA-TP is available from . CONCLUSION: Our extensive testing using simulated datasets shows that GRAPPA-TP is very accurate in terms of ancestor genome inference and phylogenetic reconstruction. Simulation results also suggest that model match is critical in genome rearrangement analysis: it is not accurate to simulate transpositions with other events including inversions.
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spelling pubmed-25598792008-10-04 Phylogenetic reconstruction from transpositions Yue, Feng Zhang, Meng Tang, Jijun BMC Genomics Research BACKGROUND: Because of the advent of high-throughput sequencing and the consequent reduction in the cost of sequencing, many organisms have been completely sequenced and most of their genes identified. It thus has become possible to represent whole genomes as ordered lists of gene identifiers and to study the rearrangement of these entities through computational means. As a result, genome rearrangement data has attracted increasing attentions from both biologists and computer scientists as a new type of data for phylogenetic analysis. The main events of genome rearrangements include inversions, transpositions and transversions. To date, GRAPPA and MGR are the most accurate methods for rearrangement phylogeny, both assuming inversion as the only event. However, due to the complexity of computing transposition distance, it is very difficult to analyze datasets when transpositions are dominant. RESULTS: We extend GRAPPA to handle transpositions. The new method is named GRAPPA-TP, with two major extensions: a heuristic method to estimate transposition distance, and a new transposition median solver for three genomes. Although GRAPPA-TP uses a greedy approach to compute the transposition distance, it is very accurate when genomes are relatively close. The new GRAPPA-TP is available from . CONCLUSION: Our extensive testing using simulated datasets shows that GRAPPA-TP is very accurate in terms of ancestor genome inference and phylogenetic reconstruction. Simulation results also suggest that model match is critical in genome rearrangement analysis: it is not accurate to simulate transpositions with other events including inversions. BioMed Central 2008-09-16 /pmc/articles/PMC2559879/ /pubmed/18831780 http://dx.doi.org/10.1186/1471-2164-9-S2-S15 Text en Copyright © 2008 Yue 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
Yue, Feng
Zhang, Meng
Tang, Jijun
Phylogenetic reconstruction from transpositions
title Phylogenetic reconstruction from transpositions
title_full Phylogenetic reconstruction from transpositions
title_fullStr Phylogenetic reconstruction from transpositions
title_full_unstemmed Phylogenetic reconstruction from transpositions
title_short Phylogenetic reconstruction from transpositions
title_sort phylogenetic reconstruction from transpositions
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2559879/
https://www.ncbi.nlm.nih.gov/pubmed/18831780
http://dx.doi.org/10.1186/1471-2164-9-S2-S15
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