Approaches to multiplicity issues in complex research in microarray analysis

被引:29
作者
Yekutieli, Daniel
Reiner-Benaim, Anat
Benjamini, Yoav
Elmer, Gregory I.
Kafkafi, Neri
Letwin, Noah E.
Lee, Norman H.
机构
[1] Tel Aviv Univ, Sackler Fac Exact Sci, Dept Stat & Operat Res, IL-61390 Tel Aviv, Israel
[2] Univ Maryland, Maryland Psychiat Res Ctr, Baltimore, MO USA
[3] George Washington Univ, Med Ctr, Washington, DC 20037 USA
[4] Inst Genom Res, Dept Funct Genom, Rockville, MD USA
关键词
false discovery rate; hierarchical testing; high throughput analysis;
D O I
10.1111/j.1467-9574.2006.00343.x
中图分类号
O21 [概率论与数理统计]; C8 [统计学];
学科分类号
020208 ; 070103 ; 0714 ;
摘要
The multiplicity problem is evident in the simplest form of statistical analysis of gene expression data - the identification of differentially expressed genes. In more complex analysis, the problem is compounded by the multiplicity of hypotheses per gene. Thus, in some cases, it may be necessary to consider testing millions of hypotheses. We present three general approaches for addressing multiplicity in large research problems. (a) Use the scalability of false discovery rate (FDR) controlling procedures; (b) apply FDR-controlling procedures to a selected subset of hypotheses; (c) apply hierarchical FDR-controlling procedures. We also offer a general framework for ensuring reproducible results in complex research, where a researcher faces more than just one large research problem. We demonstrate these approaches by analyzing the results of a complex experiment involving the study of gene expression levels in different brain regions across multiple mouse strains.
引用
收藏
页码:414 / 437
页数:24
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