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Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize

In quantitative trait locus (QTL) mapping studies, it is mandatory that the available financial resources are spent in such a way that the power for detection of QTL is maximized. The objective of this study was to optimize for three different fixed budgets the power of QTL detection 1 − β* in recom...

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Autores principales: Stich, Benjamin, Utz, H. Friedrich, Piepho, Hans-Peter, Maurer, Hans P., Melchinger, Albrecht E.
Formato: Texto
Lenguaje:English
Publicado: Springer-Verlag 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807940/
https://www.ncbi.nlm.nih.gov/pubmed/19847390
http://dx.doi.org/10.1007/s00122-009-1175-2
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author Stich, Benjamin
Utz, H. Friedrich
Piepho, Hans-Peter
Maurer, Hans P.
Melchinger, Albrecht E.
author_facet Stich, Benjamin
Utz, H. Friedrich
Piepho, Hans-Peter
Maurer, Hans P.
Melchinger, Albrecht E.
author_sort Stich, Benjamin
collection PubMed
description In quantitative trait locus (QTL) mapping studies, it is mandatory that the available financial resources are spent in such a way that the power for detection of QTL is maximized. The objective of this study was to optimize for three different fixed budgets the power of QTL detection 1 − β* in recombinant inbred line (RIL) populations derived from a nested design by varying (1) the genetic complexity of the trait, (2) the costs for developing, genotyping, and phenotyping RILs, (3) the total number of RILs, and (4) the number of environments and replications per environment used for phenotyping. Our computer simulations were based on empirical data of 653 single nucleotide polymorphism markers of 26 diverse maize inbred lines which were selected on the basis of 100 simple sequence repeat markers out of a worldwide sample of 260 maize inbreds to capture the maximum genetic diversity. For the standard scenario of costs, the optimum number of test environments (E (opt)) ranged across the examined total budgets from 7 to 19 in the scenarios with 25 QTL. In comparison, the E (opt) values observed for the scenarios with 50 and 100 QTL were slightly higher. Our finding of differences in 1 − β* estimates between experiments with optimally and sub-optimally allocated resources illustrated the potential to improve the power for QTL detection without increasing the total resources necessary for a QTL mapping experiment. Furthermore, the results of our study indicated that also in studies using the latest genomics tools to dissect quantitative traits, it is required to evaluate the individuals of the mapping population in a high number of environments with a high number of replications per environment.
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spelling pubmed-28079402010-01-22 Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize Stich, Benjamin Utz, H. Friedrich Piepho, Hans-Peter Maurer, Hans P. Melchinger, Albrecht E. Theor Appl Genet Original Paper In quantitative trait locus (QTL) mapping studies, it is mandatory that the available financial resources are spent in such a way that the power for detection of QTL is maximized. The objective of this study was to optimize for three different fixed budgets the power of QTL detection 1 − β* in recombinant inbred line (RIL) populations derived from a nested design by varying (1) the genetic complexity of the trait, (2) the costs for developing, genotyping, and phenotyping RILs, (3) the total number of RILs, and (4) the number of environments and replications per environment used for phenotyping. Our computer simulations were based on empirical data of 653 single nucleotide polymorphism markers of 26 diverse maize inbred lines which were selected on the basis of 100 simple sequence repeat markers out of a worldwide sample of 260 maize inbreds to capture the maximum genetic diversity. For the standard scenario of costs, the optimum number of test environments (E (opt)) ranged across the examined total budgets from 7 to 19 in the scenarios with 25 QTL. In comparison, the E (opt) values observed for the scenarios with 50 and 100 QTL were slightly higher. Our finding of differences in 1 − β* estimates between experiments with optimally and sub-optimally allocated resources illustrated the potential to improve the power for QTL detection without increasing the total resources necessary for a QTL mapping experiment. Furthermore, the results of our study indicated that also in studies using the latest genomics tools to dissect quantitative traits, it is required to evaluate the individuals of the mapping population in a high number of environments with a high number of replications per environment. Springer-Verlag 2009-10-22 2010 /pmc/articles/PMC2807940/ /pubmed/19847390 http://dx.doi.org/10.1007/s00122-009-1175-2 Text en © The Author(s) 2009 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
spellingShingle Original Paper
Stich, Benjamin
Utz, H. Friedrich
Piepho, Hans-Peter
Maurer, Hans P.
Melchinger, Albrecht E.
Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title_full Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title_fullStr Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title_full_unstemmed Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title_short Optimum allocation of resources for QTL detection using a nested association mapping strategy in maize
title_sort optimum allocation of resources for qtl detection using a nested association mapping strategy in maize
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2807940/
https://www.ncbi.nlm.nih.gov/pubmed/19847390
http://dx.doi.org/10.1007/s00122-009-1175-2
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