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Title: HAPRAP: a haplotype-based iterative method for statistical fine mapping using GWAS summary statistics.
Authors: Zheng, J.
Rodriguez, S.
Laurin, C.
Baird, D.
Trela-Larsen, L.
Erzurumluoglu, Mesut A.
Zheng, Y.
White, J.
Giambartolomei, C.
Zabaneh, D.
Morris, R.
Kumari, M.
Casas, J. P.
Hingorani, A. D.
UCLEB Consortium
Evans, D. M.
Gaunt, T. R.
Day, I. N.
First Published: 1-Sep-2016
Publisher: Oxford University Press (OUP)
Citation: Bioinformatics, 2016
Abstract: MOTIVATION: Fine mapping is a widely used approach for identifying the causal variant(s) at disease-associated loci. Standard methods (e.g. multiple regression) require individual level genotypes. Recent fine mapping methods using summary-level data require the pairwise correlation coefficients (r(2)) of the variants. However, haplotypes rather than pairwise r(2), are the true biological representation of linkage disequilibrium (LD) among multiple loci. In this paper, we present an empirical iterative method, HAPlotype Regional Association analysis Program (HAPRAP), that enables fine mapping using summary statistics and haplotype information from an individual-level reference panel. RESULTS: Simulations with individual-level genotypes show that the results of HAPRAP and multiple regression are highly consistent. In simulation with summary-level data, we demonstrate that HAPRAP is less sensitive to poor LD estimates. In a parametric simulation using Genetic Investigation of ANthropometric Traits (GIANT) height data, HAPRAP performs well with a small training sample size (N<2000) while other methods become suboptimal. Moreover, HAPRAP's performance is not affected substantially by SNPs with low minor allele frequencies. We applied the method to existing quantitative trait and binary outcome meta-analyses (human height, QTc interval and gallbladder disease); all previous reported association signals were replicated and two additional variants were independently associated with human height. Due to the growing availability of summary level data, the value of HAPRAP is likely to increase markedly for future analyses (e.g. functional prediction and identification of instruments for Mendelian randomization). AVAILABILITY: The HAPRAP package and documentation are available online:
DOI Link: 10.1093/bioinformatics/btw565
ISSN: 1367-4803
eISSN: 1460-2059
Version: Publisher Version
Status: Peer-reviewed
Type: Journal Article
Rights: © The Author 2016. Published by Oxford University Press. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
Appears in Collections:Published Articles, Dept. of Health Sciences

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