LD Hub: a centralized database and web interface to perform LD score regression that maximizes the potential of summary level GWAS data for SNP heritability and genetic correlation analysis

Jie Zheng(University of Bristol), A. Mesut Erzurumluoglu(University of Leicester), Benjamin Elsworth(University of Bristol), John P. Kemp(Translational Research Institute), Laurence J Howe(University of Bristol), Philip Haycock(University of Bristol), Gibran Hemani(University of Bristol), Katherine E. Tansey(University of Bristol), Charles Laurin(University of Bristol), Beaté St Pourcain(University of Bristol), Nicole M. Warrington(Translational Research Institute), Hilary K. Finucane(Harvard University), Alkes L. Price(Broad Institute), Brendan Bulik‐Sullivan(Broad Institute), Verneri Anttila(Broad Institute), Lavinia Paternoster(University of Bristol), Tom R. Gaunt(University of Bristol), David M. Evans(Translational Research Institute), Benjamin M. Neale(Broad Institute)
Bioinformatics
September 22, 2016
Cited by 1,023Open Access
Full Text

Abstract

MOTIVATION: LD score regression is a reliable and efficient method of using genome-wide association study (GWAS) summary-level results data to estimate the SNP heritability of complex traits and diseases, partition this heritability into functional categories, and estimate the genetic correlation between different phenotypes. Because the method relies on summary level results data, LD score regression is computationally tractable even for very large sample sizes. However, publicly available GWAS summary-level data are typically stored in different databases and have different formats, making it difficult to apply LD score regression to estimate genetic correlations across many different traits simultaneously. RESULTS: In this manuscript, we describe LD Hub - a centralized database of summary-level GWAS results for 173 diseases/traits from different publicly available resources/consortia and a web interface that automates the LD score regression analysis pipeline. To demonstrate functionality and validate our software, we replicated previously reported LD score regression analyses of 49 traits/diseases using LD Hub; and estimated SNP heritability and the genetic correlation across the different phenotypes. We also present new results obtained by uploading a recent atopic dermatitis GWAS meta-analysis to examine the genetic correlation between the condition and other potentially related traits. In response to the growing availability of publicly accessible GWAS summary-level results data, our database and the accompanying web interface will ensure maximal uptake of the LD score regression methodology, provide a useful database for the public dissemination of GWAS results, and provide a method for easily screening hundreds of traits for overlapping genetic aetiologies. AVAILABILITY AND IMPLEMENTATION: The web interface and instructions for using LD Hub are available at http://ldsc.broadinstitute.org/ CONTACT: jie.zheng@bristol.ac.ukSupplementary information: Supplementary data are available at Bioinformatics online.


Related Papers

No related papers found

Powered by citation graph analysis