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This article is part of the supplement: Genetic Analysis Workshop 15: Gene Expression Analysis and Approaches to Detecting Multiple Functional Loci .

Open AccessProceedings

The multiplicity problem in linkage analysis of gene expression data – the power of differentiating cis- and trans-acting regulators

Baisong Huang1,2 email, Jagadish Rangrej1 email, Andrew D Paterson1,2 email and Lei Sun1,2,3 email

Research Institute, Hospital for Sick Children, 555 University Avenue, Toronto, Ontario, M5G 1X8, Canada

Department of Public Health Sciences, University of Toronto, 155 College Street, Toronto, Ontario, M5T 3M7, Canada

Department of Statistics, University of Toronto, 100 St. George Street, Toronto, Ontario, M53 3G3, Canada

author email corresponding author email

BMC Proceedings 2007, 1(Suppl 1):S142

Published: 18 December 2007

Abstract

In this report, we focused on the multiplicity issue in Problem 1 of Genetic Analysis Workshop 15. We investigated and compared the performance of the stratified false-discovery rate control method with the traditional aggregated approach, in an application to genome-wide linkage analyses of single-nucleotide polymorphism-to-gene expression data. We showed the importance of utilizing the available map information and demonstrated the power gained by conducting false-discovery rate control separately for cis and trans regulators under three different frameworks: fixed rejection region, fixed false-discovery rate, and fixed number of rejections.


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