From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.

Unraveling the genetic background of economic traits is a major goal in modern animal genetics and breeding. Both candidate gene analysis and QTL mapping have previously been used for identifying genes and chromosome regions related to studied traits. However, most of these studies may be limited in...

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Main Authors: Minghui Wang, Qishan Wang, Yuchun Pan
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3544924?pdf=render
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spelling doaj-a557e9f8510b40548a68b67240761b3e2020-11-24T21:41:54ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0181e5345210.1371/journal.pone.0053452From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.Minghui WangQishan WangYuchun PanUnraveling the genetic background of economic traits is a major goal in modern animal genetics and breeding. Both candidate gene analysis and QTL mapping have previously been used for identifying genes and chromosome regions related to studied traits. However, most of these studies may be limited in their ability to fully consider how multiple genetic factors may influence a particular phenotype of interest. If possible, taking advantage of the combined effect of multiple genetic factors is expected to be more powerful than analyzing single sites, as the joint action of multiple loci within a gene or across multiple genes acting in the same gene set will likely have a greater influence on phenotypic variation. Thus, we proposed a pipeline of gene set analysis that utilized information from multiple loci to improve statistical power. We assessed the performance of this approach by both simulated and a real IGF1-FoxO pathway data set. The results showed that our new method can identify the association between genetic variation and phenotypic variation with higher statistical power and unravel the mechanisms of complex traits in a point of gene set. Additionally, the proposed pipeline is flexible to be extended to model complex genetic structures that include the interactions between different gene sets and between gene sets and environments.http://europepmc.org/articles/PMC3544924?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Minghui Wang
Qishan Wang
Yuchun Pan
spellingShingle Minghui Wang
Qishan Wang
Yuchun Pan
From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
PLoS ONE
author_facet Minghui Wang
Qishan Wang
Yuchun Pan
author_sort Minghui Wang
title From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
title_short From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
title_full From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
title_fullStr From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
title_full_unstemmed From QTL to QTN: candidate gene set approach and a case study in porcine IGF1-FoxO pathway.
title_sort from qtl to qtn: candidate gene set approach and a case study in porcine igf1-foxo pathway.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description Unraveling the genetic background of economic traits is a major goal in modern animal genetics and breeding. Both candidate gene analysis and QTL mapping have previously been used for identifying genes and chromosome regions related to studied traits. However, most of these studies may be limited in their ability to fully consider how multiple genetic factors may influence a particular phenotype of interest. If possible, taking advantage of the combined effect of multiple genetic factors is expected to be more powerful than analyzing single sites, as the joint action of multiple loci within a gene or across multiple genes acting in the same gene set will likely have a greater influence on phenotypic variation. Thus, we proposed a pipeline of gene set analysis that utilized information from multiple loci to improve statistical power. We assessed the performance of this approach by both simulated and a real IGF1-FoxO pathway data set. The results showed that our new method can identify the association between genetic variation and phenotypic variation with higher statistical power and unravel the mechanisms of complex traits in a point of gene set. Additionally, the proposed pipeline is flexible to be extended to model complex genetic structures that include the interactions between different gene sets and between gene sets and environments.
url http://europepmc.org/articles/PMC3544924?pdf=render
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AT qishanwang fromqtltoqtncandidategenesetapproachandacasestudyinporcineigf1foxopathway
AT yuchunpan fromqtltoqtncandidategenesetapproachandacasestudyinporcineigf1foxopathway
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