Extracting binary signals from microarray time-course data

被引:108
作者
Sahoo, Debashis
Dill, David L. [1 ]
Tibshirani, Rob
Plevritis, Sylvia K.
机构
[1] Stanford Univ, Dept Elect Engn, Stanford, CA 94305 USA
[2] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Radiol, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Hlth Res & Policy, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Stat, Stanford, CA 94305 USA
关键词
D O I
10.1093/nar/gkm284
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This article presents a new method for analyzing microarray time courses by identifying genes that undergo abrupt transitions in expression level, and the time at which the transitions occur. The algorithm matches the sequence of expression levels for each gene against temporal patterns having one or two transitions between two expression levels. The algorithm reports a P-value for the matching pattern of each gene, and a global false discovery rate can also be computed. After matching, genes can be sorted by the direction and time of transitions. Genes can be partitioned into sets based on the direction and time of change for further analysis, such as comparison with Gene Ontology annotations or binding site motifs. The method is evaluated on simulated and actual timecourse data. On microarray data for budding yeast, it is shown that the groups of genes that change in similar ways and at similar times have significant and relevant Gene Ontology annotations.
引用
收藏
页码:3705 / 3712
页数:8
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