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A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL

BACKGROUND: Identity by descent (IBD) matrix estimation is a central component in mapping of Quantitative Trait Loci (QTL) using variance component models. A large number of algorithms have been developed for estimation of IBD between individuals in populations at discrete locations in the genome fo...

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Autores principales: Besnier, Francois, Carlborg, Örjan
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194736/
https://www.ncbi.nlm.nih.gov/pubmed/17999749
http://dx.doi.org/10.1186/1471-2105-8-440
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author Besnier, Francois
Carlborg, Örjan
author_facet Besnier, Francois
Carlborg, Örjan
author_sort Besnier, Francois
collection PubMed
description BACKGROUND: Identity by descent (IBD) matrix estimation is a central component in mapping of Quantitative Trait Loci (QTL) using variance component models. A large number of algorithms have been developed for estimation of IBD between individuals in populations at discrete locations in the genome for use in genome scans to detect QTL affecting various traits of interest in experimental animal, human and agricultural pedigrees. Here, we propose a new approach to estimate IBD as continuous functions rather than as discrete values. RESULTS: Estimation of IBD functions improved the computational efficiency and memory usage in genome scanning for QTL. We have explored two approaches to obtain continuous marker-bracket IBD-functions. By re-implementing an existing and fast deterministic IBD-estimation method, we show that this approach results in IBD functions that produces the exact same IBD as the original algorithm, but with a greater than 2-fold improvement of the computational efficiency and a considerably lower memory requirement for storing the resulting genome-wide IBD. By developing a general IBD function approximation algorithm, we show that it is possible to estimate marker-bracket IBD functions from IBD matrices estimated at marker locations by any existing IBD estimation algorithm. The general algorithm provides approximations that lead to QTL variance component estimates that even in worst-case scenarios are very similar to the true values. The approach of storing IBD as polynomial IBD-function was also shown to reduce the amount of memory required in genome scans for QTL. CONCLUSION: In addition to direct improvements in computational and memory efficiency, estimation of IBD-functions is a fundamental step needed to develop and implement new efficient optimization algorithms for high precision localization of QTL. Here, we discuss and test two approaches for estimating IBD functions based on existing IBD estimation algorithms. Our approaches provide immediately useful techniques for use in single QTL analyses in the variance component QTL mapping framework. They will, however, be particularly useful in genome scans for multiple interacting QTL, where the improvements in both computational and memory efficiency are the key for successful development of efficient optimization algorithms to allow widespread use of this methodology.
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spelling pubmed-21947362008-01-14 A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL Besnier, Francois Carlborg, Örjan BMC Bioinformatics Methodology Article BACKGROUND: Identity by descent (IBD) matrix estimation is a central component in mapping of Quantitative Trait Loci (QTL) using variance component models. A large number of algorithms have been developed for estimation of IBD between individuals in populations at discrete locations in the genome for use in genome scans to detect QTL affecting various traits of interest in experimental animal, human and agricultural pedigrees. Here, we propose a new approach to estimate IBD as continuous functions rather than as discrete values. RESULTS: Estimation of IBD functions improved the computational efficiency and memory usage in genome scanning for QTL. We have explored two approaches to obtain continuous marker-bracket IBD-functions. By re-implementing an existing and fast deterministic IBD-estimation method, we show that this approach results in IBD functions that produces the exact same IBD as the original algorithm, but with a greater than 2-fold improvement of the computational efficiency and a considerably lower memory requirement for storing the resulting genome-wide IBD. By developing a general IBD function approximation algorithm, we show that it is possible to estimate marker-bracket IBD functions from IBD matrices estimated at marker locations by any existing IBD estimation algorithm. The general algorithm provides approximations that lead to QTL variance component estimates that even in worst-case scenarios are very similar to the true values. The approach of storing IBD as polynomial IBD-function was also shown to reduce the amount of memory required in genome scans for QTL. CONCLUSION: In addition to direct improvements in computational and memory efficiency, estimation of IBD-functions is a fundamental step needed to develop and implement new efficient optimization algorithms for high precision localization of QTL. Here, we discuss and test two approaches for estimating IBD functions based on existing IBD estimation algorithms. Our approaches provide immediately useful techniques for use in single QTL analyses in the variance component QTL mapping framework. They will, however, be particularly useful in genome scans for multiple interacting QTL, where the improvements in both computational and memory efficiency are the key for successful development of efficient optimization algorithms to allow widespread use of this methodology. BioMed Central 2007-11-13 /pmc/articles/PMC2194736/ /pubmed/17999749 http://dx.doi.org/10.1186/1471-2105-8-440 Text en Copyright © 2007 Besnier and Carlborg; 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 Methodology Article
Besnier, Francois
Carlborg, Örjan
A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title_full A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title_fullStr A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title_full_unstemmed A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title_short A general and efficient method for estimating continuous IBD functions for use in genome scans for QTL
title_sort general and efficient method for estimating continuous ibd functions for use in genome scans for qtl
topic Methodology Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2194736/
https://www.ncbi.nlm.nih.gov/pubmed/17999749
http://dx.doi.org/10.1186/1471-2105-8-440
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