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Functional group-based linkage analysis of gene expression trait loci
We explored approaches to using multiple related traits (gene expression levels) in linkage analysis. We first grouped mRNA transcripts according to their functions annotated in biological process of gene ontology (GO). We then compared using sample average, principal-components analysis (PCA), and...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367612/ https://www.ncbi.nlm.nih.gov/pubmed/18466458 |
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author | Li, Na Wu, Baolin Wei, Peng Xie, Benhuai Xie, Yang Xiao, Guanghua Pan, Wei |
author_facet | Li, Na Wu, Baolin Wei, Peng Xie, Benhuai Xie, Yang Xiao, Guanghua Pan, Wei |
author_sort | Li, Na |
collection | PubMed |
description | We explored approaches to using multiple related traits (gene expression levels) in linkage analysis. We first grouped mRNA transcripts according to their functions annotated in biological process of gene ontology (GO). We then compared using sample average, principal-components analysis (PCA), and linear discriminant analysis (LDA) to derive a univariate composite trait. Our results showed that PCA generally yielded stronger evidence for linkage, through the LDA component had the highest heritability. We also developed an algorithm to search for clusters of linkage peaks from multiple traits in the same group and a heuristic method for calculating p-value evaluating the linkage peak clustering. Future research is needed to develop rigorous methods in mapping of genes affecting the expression of a group of transcripts. |
format | Text |
id | pubmed-2367612 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23676122008-05-06 Functional group-based linkage analysis of gene expression trait loci Li, Na Wu, Baolin Wei, Peng Xie, Benhuai Xie, Yang Xiao, Guanghua Pan, Wei BMC Proc Proceedings We explored approaches to using multiple related traits (gene expression levels) in linkage analysis. We first grouped mRNA transcripts according to their functions annotated in biological process of gene ontology (GO). We then compared using sample average, principal-components analysis (PCA), and linear discriminant analysis (LDA) to derive a univariate composite trait. Our results showed that PCA generally yielded stronger evidence for linkage, through the LDA component had the highest heritability. We also developed an algorithm to search for clusters of linkage peaks from multiple traits in the same group and a heuristic method for calculating p-value evaluating the linkage peak clustering. Future research is needed to develop rigorous methods in mapping of genes affecting the expression of a group of transcripts. BioMed Central 2007-12-18 /pmc/articles/PMC2367612/ /pubmed/18466458 Text en Copyright © 2007 Li et al; 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 | Proceedings Li, Na Wu, Baolin Wei, Peng Xie, Benhuai Xie, Yang Xiao, Guanghua Pan, Wei Functional group-based linkage analysis of gene expression trait loci |
title | Functional group-based linkage analysis of gene expression trait loci |
title_full | Functional group-based linkage analysis of gene expression trait loci |
title_fullStr | Functional group-based linkage analysis of gene expression trait loci |
title_full_unstemmed | Functional group-based linkage analysis of gene expression trait loci |
title_short | Functional group-based linkage analysis of gene expression trait loci |
title_sort | functional group-based linkage analysis of gene expression trait loci |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2367612/ https://www.ncbi.nlm.nih.gov/pubmed/18466458 |
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