Cancer Outlier Analysis Based on Mixture Modeling of Gene Expression Data

被引:4
|
作者
Mori, Keita [1 ,2 ]
Oura, Tomonori [3 ]
Noma, Hisashi [4 ]
Matsui, Shigeyuki [1 ,4 ]
机构
[1] Grad Univ Adv Studies, Dept Stat Sci, Sch Multidisciplinary Sci, Tachikawa, Tokyo 1908562, Japan
[2] Shizuoka Canc Ctr, Clin Trial Coordinat Off, Nagaizumi, Shizuoka 4118777, Japan
[3] Eli Lilly Japan, Asia Pacific Stat Sci, Lilly Res Labs, Dev Ctr Excellence Asia Pacific,Chuo Ku, Kobe, Hyogo 6510086, Japan
[4] Inst Stat Math, Dept Data Sci, Tachikawa, Tokyo 1908562, Japan
关键词
SAMPLE-SIZE; FDR-CONTROL; FUSION;
D O I
10.1155/2013/693901
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Molecular heterogeneity of cancer, partially caused by various chromosomal aberrations or gene mutations, can yield substantial heterogeneity in gene expression profile in cancer samples. To detect cancer-related genes which are active only in a subset of cancer samples or cancer outliers, several methods have been proposed in the context of multiple testing. Such cancer outlier analyses will generally suffer from a serious lack of power, compared with the standard multiple testing setting where common activation of genes across all cancer samples is supposed. In this paper, we consider information sharing across genes and cancer samples, via a parametric normal mixture modeling of gene expression levels of cancer samples across genes after a standardization using the reference, normal sample data. A gene-based statistic for gene selection is developed on the basis of a posterior probability of cancer outlier for each cancer sample. Some efficiency improvement by using our method was demonstrated, even under settings with misspecified, heavy-tailed t-distributions. An application to a real dataset from hematologic malignancies is provided.
引用
收藏
页数:8
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