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Author(s):
Corbin Quick, Christian Fuchsberger, Daniel Taliun, Gonçalo Abecasis, Michael Boehnke, Hyun Min Kang
Publish date:
2 July 2018
Journal:
Bioinformatics
PubMed ID:
30204848

Abstract

Summary: Estimating linkage disequilibrium (LD) is essential for a wide range of summary statistics-based association methods for genome-wide association studies. Large genetic datasets, e.g. the TOPMed WGS project and UK Biobank, enable more accurate and comprehensive LD estimates, but increase the computational burden of LD estimation. Here, we describe emeraLD (Efficient Methods for Estimation and Random Access of LD), a computational tool that leverages sparsity and haplotype structure to estimate LD up to 2 orders of magnitude faster than current tools.

Availability and implementation: emeraLD is implemented in C++, and is open source under GPLv3. Source code and documentation are freely available at http://github.com/statgen/emeraLD.

Supplementary information: Supplementary data are available at Bioinformatics online.

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We aim to identify novel genetic markers of complex human traits, including a number of psychiatric, ocular, dermatological, and cardiovascular diseases. In particular we hope…

Institution:
University of Michigan, United States of America

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