Mapping gene expression quantitative trait loci by singular value decomposition and independent component analysis.
Mapping gene expression quantitative trait loci by singular value decomposition and independent component analysis.
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通过单数值分解和独立的成分分析来映射基因表达定量特质基因座。
DOI:
10.1186/1471-2105-9-244
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发表时间:
2008-05-20
影响因子:
3
通讯作者:
Akey, Joshua M.
中科院分区:
文献类型:
--
作者:
Biswas, Shameek;Storey, John D.;Akey, Joshua M.
The combination of gene expression profiling with linkage analysis has become a powerful paradigm for mapping gene expression quantitative trait loci (eQTL). To date, most studies have searched for eQTL by analyzing gene expression traits one at a time. As thousands of expression traits are typically analyzed, this can reduce power because of the need to correct for the number of hypothesis tests performed. In addition, gene expression traits exhibit a complex correlation structure, which is ignored when analyzing traits individually. To address these issues, we applied two different multivariate dimension reduction techniques, the Singular Value Decomposition (SVD) and Independent Component Analysis (ICA) to gene expression traits derived from a cross between two strains of Saccharomyces cerevisiae. Both methods decompose the data into a set of meta-traits, which are linear combinations of all the expression traits. The meta-traits were enriched for several Gene Ontology categories including metabolic pathways, stress response, RNA processing, ion transport, retro-transposition and telomeric maintenance. Genome-wide linkage analysis was performed on the top 20 meta-traits from both techniques. In total, 21 eQTL were found, of which 11 are novel. Interestingly, both cis and trans-linkages to the meta-traits were observed. These results demonstrate that dimension reduction methods are a useful and complementary approach for probing the genetic architecture of gene expression variation.
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影响因子:
12.3
作者:
Lee SI;Batzoglou S
通讯作者:
Batzoglou S
影响因子:
2.9
作者:
Bensen, JT;Lange, LA;Langefeld, CD;Chang, BL;Bleecker, ER;Meyers, DA;Xu, JF
通讯作者:
Xu, JF
影响因子:
3
作者:
Frigyesi A;Veerla S;Lindgren D;Höglund M
通讯作者:
Höglund M
影响因子:
7.8
作者:
Hyvärinen, A;Oja, E
通讯作者:
Oja, E
影响因子:
3.3
作者:
Bing, N;Hoeschele, I
通讯作者:
Hoeschele, I