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Minimizing recombinations in consensus networks for phylogeographic studies
BACKGROUND: We address the problem of studying recombinational variations in (human) populations. In this paper, our focus is on one computational aspect of the general task: Given two networks G(1 )and G(2), with both mutation and recombination events, defined on overlapping sets of extant units th...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648726/ https://www.ncbi.nlm.nih.gov/pubmed/19208177 http://dx.doi.org/10.1186/1471-2105-10-S1-S72 |
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author | Parida, Laxmi Javed, Asif Melé, Marta Calafell, Francesc Bertranpetit, Jaume |
author_facet | Parida, Laxmi Javed, Asif Melé, Marta Calafell, Francesc Bertranpetit, Jaume |
author_sort | Parida, Laxmi |
collection | PubMed |
description | BACKGROUND: We address the problem of studying recombinational variations in (human) populations. In this paper, our focus is on one computational aspect of the general task: Given two networks G(1 )and G(2), with both mutation and recombination events, defined on overlapping sets of extant units the objective is to compute a consensus network G(3 )with minimum number of additional recombinations. We describe a polynomial time algorithm with a guarantee that the number of computed new recombination events is within ϵ = sz(G(1), G(2)) (function sz is a well-behaved function of the sizes and topologies of G(1 )and G(2)) of the optimal number of recombinations. To date, this is the best known result for a network consensus problem. RESULTS: Although the network consensus problem can be applied to a variety of domains, here we focus on structure of human populations. With our preliminary analysis on a segment of the human Chromosome X data we are able to infer ancient recombinations, population-specific recombinations and more, which also support the widely accepted 'Out of Africa' model. These results have been verified independently using traditional manual procedures. To the best of our knowledge, this is the first recombinations-based characterization of human populations. CONCLUSION: We show that our mathematical model identifies recombination spots in the individual haplotypes; the aggregate of these spots over a set of haplotypes defines a recombinational landscape that has enough signal to detect continental as well as population divide based on a short segment of Chromosome X. In particular, we are able to infer ancient recombinations, population-specific recombinations and more, which also support the widely accepted 'Out of Africa' model. The agreement with mutation-based analysis can be viewed as an indirect validation of our results and the model. Since the model in principle gives us more information embedded in the networks, in our future work, we plan to investigate more non-traditional questions via these structures computed by our methodology. |
format | Text |
id | pubmed-2648726 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26487262009-03-03 Minimizing recombinations in consensus networks for phylogeographic studies Parida, Laxmi Javed, Asif Melé, Marta Calafell, Francesc Bertranpetit, Jaume BMC Bioinformatics Research BACKGROUND: We address the problem of studying recombinational variations in (human) populations. In this paper, our focus is on one computational aspect of the general task: Given two networks G(1 )and G(2), with both mutation and recombination events, defined on overlapping sets of extant units the objective is to compute a consensus network G(3 )with minimum number of additional recombinations. We describe a polynomial time algorithm with a guarantee that the number of computed new recombination events is within ϵ = sz(G(1), G(2)) (function sz is a well-behaved function of the sizes and topologies of G(1 )and G(2)) of the optimal number of recombinations. To date, this is the best known result for a network consensus problem. RESULTS: Although the network consensus problem can be applied to a variety of domains, here we focus on structure of human populations. With our preliminary analysis on a segment of the human Chromosome X data we are able to infer ancient recombinations, population-specific recombinations and more, which also support the widely accepted 'Out of Africa' model. These results have been verified independently using traditional manual procedures. To the best of our knowledge, this is the first recombinations-based characterization of human populations. CONCLUSION: We show that our mathematical model identifies recombination spots in the individual haplotypes; the aggregate of these spots over a set of haplotypes defines a recombinational landscape that has enough signal to detect continental as well as population divide based on a short segment of Chromosome X. In particular, we are able to infer ancient recombinations, population-specific recombinations and more, which also support the widely accepted 'Out of Africa' model. The agreement with mutation-based analysis can be viewed as an indirect validation of our results and the model. Since the model in principle gives us more information embedded in the networks, in our future work, we plan to investigate more non-traditional questions via these structures computed by our methodology. BioMed Central 2009-01-30 /pmc/articles/PMC2648726/ /pubmed/19208177 http://dx.doi.org/10.1186/1471-2105-10-S1-S72 Text en Copyright © 2009 Parida 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 Parida, Laxmi Javed, Asif Melé, Marta Calafell, Francesc Bertranpetit, Jaume Minimizing recombinations in consensus networks for phylogeographic studies |
title | Minimizing recombinations in consensus networks for phylogeographic studies |
title_full | Minimizing recombinations in consensus networks for phylogeographic studies |
title_fullStr | Minimizing recombinations in consensus networks for phylogeographic studies |
title_full_unstemmed | Minimizing recombinations in consensus networks for phylogeographic studies |
title_short | Minimizing recombinations in consensus networks for phylogeographic studies |
title_sort | minimizing recombinations in consensus networks for phylogeographic studies |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2648726/ https://www.ncbi.nlm.nih.gov/pubmed/19208177 http://dx.doi.org/10.1186/1471-2105-10-S1-S72 |
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