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Testing Pleiotropy vs. Separate QTL in Multiparental Populations

The high mapping resolution of multiparental populations, combined with technology to measure tens of thousands of phenotypes, presents a need for quantitative methods to enhance understanding of the genetic architecture of complex traits. When multiple traits map to a common genomic region, knowled...

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Detalles Bibliográficos
Autores principales: Boehm, Frederick J., Chesler, Elissa J., Yandell, Brian S., Broman, Karl W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643884/
https://www.ncbi.nlm.nih.gov/pubmed/31092608
http://dx.doi.org/10.1534/g3.119.400098
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author Boehm, Frederick J.
Chesler, Elissa J.
Yandell, Brian S.
Broman, Karl W.
author_facet Boehm, Frederick J.
Chesler, Elissa J.
Yandell, Brian S.
Broman, Karl W.
author_sort Boehm, Frederick J.
collection PubMed
description The high mapping resolution of multiparental populations, combined with technology to measure tens of thousands of phenotypes, presents a need for quantitative methods to enhance understanding of the genetic architecture of complex traits. When multiple traits map to a common genomic region, knowledge of the number of distinct loci provides important insight into the underlying mechanism and can assist planning for subsequent experiments. We extend the method of Jiang and Zeng (1995), for testing pleiotropy with a pair of traits, to the case of more than two alleles. We also incorporate polygenic random effects to account for population structure. We use a parametric bootstrap to determine statistical significance. We apply our methods to a behavioral genetics data set from Diversity Outbred mice. Our methods have been incorporated into the R package qtl2pleio.
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spelling pubmed-66438842019-07-25 Testing Pleiotropy vs. Separate QTL in Multiparental Populations Boehm, Frederick J. Chesler, Elissa J. Yandell, Brian S. Broman, Karl W. G3 (Bethesda) Multiparental Populations The high mapping resolution of multiparental populations, combined with technology to measure tens of thousands of phenotypes, presents a need for quantitative methods to enhance understanding of the genetic architecture of complex traits. When multiple traits map to a common genomic region, knowledge of the number of distinct loci provides important insight into the underlying mechanism and can assist planning for subsequent experiments. We extend the method of Jiang and Zeng (1995), for testing pleiotropy with a pair of traits, to the case of more than two alleles. We also incorporate polygenic random effects to account for population structure. We use a parametric bootstrap to determine statistical significance. We apply our methods to a behavioral genetics data set from Diversity Outbred mice. Our methods have been incorporated into the R package qtl2pleio. Genetics Society of America 2019-05-15 /pmc/articles/PMC6643884/ /pubmed/31092608 http://dx.doi.org/10.1534/g3.119.400098 Text en Copyright © 2019 Boehm et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Multiparental Populations
Boehm, Frederick J.
Chesler, Elissa J.
Yandell, Brian S.
Broman, Karl W.
Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title_full Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title_fullStr Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title_full_unstemmed Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title_short Testing Pleiotropy vs. Separate QTL in Multiparental Populations
title_sort testing pleiotropy vs. separate qtl in multiparental populations
topic Multiparental Populations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6643884/
https://www.ncbi.nlm.nih.gov/pubmed/31092608
http://dx.doi.org/10.1534/g3.119.400098
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