fcfdr: an R package to leverage continuous and binary functional genomic data in GWAS
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Peer-reviewed
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Authors
Hutchinson, Anna https://orcid.org/0000-0002-9224-4410
Liley, James
Wallace, Chris https://orcid.org/0000-0001-9755-1703
Abstract
Summary
GWAS discovery is limited in power to detect associations that exceed the stringent genome-wide significance threshold, but this limitation can be alleviated by leveraging relevant auxiliary data. Frameworks utilising the conditional false discovery rate (cFDR) can be used to leverage continuous auxiliary data (including GWAS and functional genomic data) with GWAS test statistics and have been shown to increase power for GWAS discovery whilst controlling the FDR. Here, we describe an extension to the cFDR framework for binary auxiliary data (such as whether SNPs reside in regions of the genome with specific activity states) and introduce an all-encompassing R package to implement the cFDR approach, fcfdr , demonstrating its utility in an application to type 1 diabetes.Availability and implementation
The fcfdr R package is freely available at: https://github.com/annahutch/fcfdr . Scripts and data to reproduce the analysis in this paper are freely available at: https://annahutch.github.io/fcfdr/articles/t1d_app.htmlDescription
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Journal Title
BMC Bioinformatics
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1471-2105
1471-2105
1471-2105
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BioMed Central
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Sponsorship
Medical Research Council (MC_UU_00002/4)