Statistical analysis of big data on pharmacogenomics

被引:41
作者
Fan, Jianqing [1 ]
Liu, Han [1 ]
机构
[1] Princeton Univ, Dept Operat Res & Financial Engn, Princeton, NJ 08544 USA
基金
美国国家科学基金会;
关键词
Big data; High dimensional statistics; Approximate factor model; Graphical model; Multiple testing; Variable selection; Marginal screening; Robust statistics; NONCONCAVE PENALIZED LIKELIHOOD; COVARIANCE-MATRIX ESTIMATION; FALSE DISCOVERY RATE; GENERALIZED LINEAR-MODELS; VARIABLE SELECTION; THRESHOLDING ALGORITHM; REGULARIZATION; CLASSIFICATION; REGRESSION; SHRINKAGE;
D O I
10.1016/j.addr.2013.04.008
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
This paper discusses statistical methods for estimating complex correlation structure from large pharmacogenomic datasets. We selectively review several prominent statistical methods for estimating large covariance matrix for understanding correlation structure, inverse covariance matrix for network modeling, large-scale simultaneous tests for selecting significantly differently expressed genes and proteins and generic markers for complex diseases, and high dimensional variable selection for identifying important molecules for understanding molecule mechanisms in pharmacogenomics. Their applications to gene network estimation and biomarker selection are used to illustrate the methodological power. Several new challenges of Big data analysis, including complex data distribution, missing data, measurement error, spurious correlation, endogeneity, and the need for robust statistical methods, are also discussed. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:987 / 1000
页数:14
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