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Pathway-directed weighted testing procedures for the integrative analysis of gene expression and metabolomic data
被引:10
|作者:
Poisson, Laila M.
[1
]
Sreekumar, Arun
[2
]
Chinnaiyan, Arul M.
[3
]
Ghosh, Debashis
[4
,5
]
机构:
[1] Henry Ford Hosp, Dept Publ Hlth Sci, Detroit, MI 48202 USA
[2] Baylor Coll Med, Alkek Ctr Mol Discovery, Houston, TX 77030 USA
[3] Univ Michigan, Michigan Ctr Translat Pathol, Ann Arbor, MI 48109 USA
[4] Penn State Univ, Dept Stat, University Pk, PA 16802 USA
[5] Penn State Univ, Dept Publ Hlth Sci, University Pk, PA USA
来源:
关键词:
Cancer;
Metabolomic data;
Multiple testing;
Pathway information;
Transcriptomic data;
GENOMICS;
CANCER;
VISUALIZATION;
PROTEOMICS;
PROFILES;
TOOL;
D O I:
10.1016/j.ygeno.2012.03.004
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
We explore the utility of p-value weighting for enhancing the power to detect differential metabolites in a two-sample setting. Related gene expression information is used to assign an a priori importance level to each metabolite being tested. We map the gene expression to a metabolite through pathways and then gene expression information is summarized per-pathway using gene set enrichment tests. Through simulation we explore four styles of enrichment tests and four weight functions to convert the gene information into a meaningful p-value weight. We implement the p-value weighting on a prostate cancer metabolomic dataset. Gene expression on matched samples is used to construct the weights. Under certain regulatory conditions, the use of weighted p-values does not inflate the type 1 error above what we see for the un-weighted tests except in high correlation situations. The power to detect differential metabolites is notably increased in situations with disjoint pathways and shows moderate improvement, relative to the proportion of enriched pathways, when pathway membership overlaps. (C) 2012 Elsevier Inc. All rights reserved.
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页码:265 / 274
页数:10
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