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Power of QTL detection by either fixed or random models in half-sib designs
The aim of this study was to compare the variance component approach for QTL linkage mapping in half-sib designs to the simple regression method. Empirical power was determined by Monte Carlo simulation in granddaughter designs. The factors studied (base values in parentheses) included the number of...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697240/ https://www.ncbi.nlm.nih.gov/pubmed/16277970 http://dx.doi.org/10.1186/1297-9686-37-7-601 |
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author | Kolbehdari, Davood Jansen, Gerald B Schaeffer, Lawrence R Allen, Brian O |
author_facet | Kolbehdari, Davood Jansen, Gerald B Schaeffer, Lawrence R Allen, Brian O |
author_sort | Kolbehdari, Davood |
collection | PubMed |
description | The aim of this study was to compare the variance component approach for QTL linkage mapping in half-sib designs to the simple regression method. Empirical power was determined by Monte Carlo simulation in granddaughter designs. The factors studied (base values in parentheses) included the number of sires (5) and sons per sire (80), ratio of QTL variance to total genetic variance (λ = 0.1), marker spacing (10 cM), and QTL allele frequency (0.5). A single bi-allelic QTL and six equally spaced markers with six alleles each were simulated. Empirical power using the regression method was 0.80, 0.92 and 0.98 for 5, 10, and 20 sires, respectively, versus 0.88, 0.98 and 0.99 using the variance component method. Power was 0.74, 0.80, 0.93, and 0.95 using regression versus 0.77, 0.88, 0.94, and 0.97 using the variance component method for QTL variance ratios (λ) of 0.05, 0.1, 0.2, and 0.3, respectively. Power was 0.79, 0.85, 0.80 and 0.87 using regression versus 0.80, 0.86, 0.88, and 0.85 using the variance component method for QTL allele frequencies of 0.1, 0.3, 0.5, and 0.8, respectively. The log(10 )of type I error profiles were quite flat at close marker spacing (1 cM), confirming the inability to fine-map QTL by linkage analysis in half-sib designs. The variance component method showed slightly more potential than the regression method in QTL mapping. |
format | Text |
id | pubmed-2697240 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-26972402009-06-16 Power of QTL detection by either fixed or random models in half-sib designs Kolbehdari, Davood Jansen, Gerald B Schaeffer, Lawrence R Allen, Brian O Genet Sel Evol Research The aim of this study was to compare the variance component approach for QTL linkage mapping in half-sib designs to the simple regression method. Empirical power was determined by Monte Carlo simulation in granddaughter designs. The factors studied (base values in parentheses) included the number of sires (5) and sons per sire (80), ratio of QTL variance to total genetic variance (λ = 0.1), marker spacing (10 cM), and QTL allele frequency (0.5). A single bi-allelic QTL and six equally spaced markers with six alleles each were simulated. Empirical power using the regression method was 0.80, 0.92 and 0.98 for 5, 10, and 20 sires, respectively, versus 0.88, 0.98 and 0.99 using the variance component method. Power was 0.74, 0.80, 0.93, and 0.95 using regression versus 0.77, 0.88, 0.94, and 0.97 using the variance component method for QTL variance ratios (λ) of 0.05, 0.1, 0.2, and 0.3, respectively. Power was 0.79, 0.85, 0.80 and 0.87 using regression versus 0.80, 0.86, 0.88, and 0.85 using the variance component method for QTL allele frequencies of 0.1, 0.3, 0.5, and 0.8, respectively. The log(10 )of type I error profiles were quite flat at close marker spacing (1 cM), confirming the inability to fine-map QTL by linkage analysis in half-sib designs. The variance component method showed slightly more potential than the regression method in QTL mapping. BioMed Central 2005-11-15 /pmc/articles/PMC2697240/ /pubmed/16277970 http://dx.doi.org/10.1186/1297-9686-37-7-601 Text en Copyright © 2005 INRA, EDP Sciences |
spellingShingle | Research Kolbehdari, Davood Jansen, Gerald B Schaeffer, Lawrence R Allen, Brian O Power of QTL detection by either fixed or random models in half-sib designs |
title | Power of QTL detection by either fixed or random models in half-sib designs |
title_full | Power of QTL detection by either fixed or random models in half-sib designs |
title_fullStr | Power of QTL detection by either fixed or random models in half-sib designs |
title_full_unstemmed | Power of QTL detection by either fixed or random models in half-sib designs |
title_short | Power of QTL detection by either fixed or random models in half-sib designs |
title_sort | power of qtl detection by either fixed or random models in half-sib designs |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2697240/ https://www.ncbi.nlm.nih.gov/pubmed/16277970 http://dx.doi.org/10.1186/1297-9686-37-7-601 |
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