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A modified generalized Fisher method for combining probabilities from dependent tests

Overview of attention for article published in Frontiers in Genetics, January 2014
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Title
A modified generalized Fisher method for combining probabilities from dependent tests
Published in
Frontiers in Genetics, January 2014
DOI 10.3389/fgene.2014.00032
Pubmed ID
Authors

Hongying Dai, J. Steven Leeder, Yuehua Cui

Abstract

Rapid developments in molecular technology have yielded a large amount of high throughput genetic data to understand the mechanism for complex traits. The increase of genetic variants requires hundreds and thousands of statistical tests to be performed simultaneously in analysis, which poses a challenge to control the overall Type I error rate. Combining p-values from multiple hypothesis testing has shown promise for aggregating effects in high-dimensional genetic data analysis. Several p-value combining methods have been developed and applied to genetic data; see Dai et al. (2012b) for a comprehensive review. However, there is a lack of investigations conducted for dependent genetic data, especially for weighted p-value combining methods. Single nucleotide polymorphisms (SNPs) are often correlated due to linkage disequilibrium (LD). Other genetic data, including variants from next generation sequencing, gene expression levels measured by microarray, protein and DNA methylation data, etc. also contain complex correlation structures. Ignoring correlation structures among genetic variants may lead to severe inflation of Type I error rates for omnibus testing of p-values. In this work, we propose modifications to the Lancaster procedure by taking the correlation structure among p-values into account. The weight function in the Lancaster procedure allows meaningful biological information to be incorporated into the statistical analysis, which can increase the power of the statistical testing and/or remove the bias in the process. Extensive empirical assessments demonstrate that the modified Lancaster procedure largely reduces the Type I error rates due to correlation among p-values, and retains considerable power to detect signals among p-values. We applied our method to reassess published renal transplant data, and identified a novel association between B cell pathways and allograft tolerance.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 113 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
United States 2 2%
Netherlands 1 <1%
Hungary 1 <1%
United Kingdom 1 <1%
Australia 1 <1%
Unknown 107 95%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 34 30%
Researcher 21 19%
Student > Master 11 10%
Student > Bachelor 9 8%
Other 8 7%
Other 11 10%
Unknown 19 17%
Readers by discipline Count As %
Agricultural and Biological Sciences 27 24%
Biochemistry, Genetics and Molecular Biology 26 23%
Mathematics 11 10%
Computer Science 7 6%
Medicine and Dentistry 6 5%
Other 14 12%
Unknown 22 19%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 20 February 2014.
All research outputs
#20,221,866
of 22,745,803 outputs
Outputs from Frontiers in Genetics
#8,551
of 11,758 outputs
Outputs of similar age
#264,757
of 305,223 outputs
Outputs of similar age from Frontiers in Genetics
#47
of 54 outputs
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