Integrating genetic and gene expression data: methods and applications of eQTL mapping

The availability of high-throughput genotyping technologies and microarray assays has allowed researchers to investigate genetic variations that influence levels of gene expression. Expression Quantitative Trait Locus (eQTL) mapping methods have been used to identify the genetic basis of gene expres...

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Vydáno v:Yíchuán Ročník 30; číslo 9; s. 1228
Hlavní autoři: Liu, Gang, Peng, Hui-Ru, Ni, Zhong-Fu, Qin, Dan-Dan, Song, Fang-Wei, Song, Guang-Shu, Sun, Qi-Xin
Médium: Journal Article
Jazyk:čínština
Vydáno: China 01.09.2008
Témata:
Animals
Chromosome Mapping
Gene Expression - physiology
Gene Expression Profiling
Mice
Models, Genetic
Oligonucleotide Array Sequence Analysis - instrumentation
Oligonucleotide Array Sequence Analysis - methods
Quantitative Trait Loci - genetics
Quantitative Trait Loci - physiology
ISSN:0253-9772
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Shrnutí:The availability of high-throughput genotyping technologies and microarray assays has allowed researchers to investigate genetic variations that influence levels of gene expression. Expression Quantitative Trait Locus (eQTL) mapping methods have been used to identify the genetic basis of gene expression. Similar to traditional QTL studies, the main goal of eQTL is to identify the genomic locations to which the expression traits are linked. Although microarrays provide the expression data of thousands of transcripts, standard QTL mapping methods, which are able to handle at most tens of traits, cannot be applied directly. As a result, it is necessary to consider the statistical principles involved in the design and analysis of these experiments. In this paper, we reviewed individual selection, experimental design of microarray, normalization of gene expression data, mapping methods, and explaining of results and proposed potential methodological problems for such analyses. Finally, we discussed the application
Bibliografie:ObjectType-Article-2
SourceType-Scholarly Journals-1
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content type line 23
ISSN:0253-9772
DOI:10.3724/sp.j.1005.2008.01228