Journal article
Identity-by-Descent Mapping to Detect Rare Variants Conferring Susceptibility to Multiple Sclerosis
R Lin, J Charlesworth, J Stankovich, VM Perreau, MA Brown, A Baxter, A Kermode, M Bahlo, W Carroll, H Butzkueven, D Booth, G Stewart, J Wiley, J Field, L Tajouri, L Griffiths, M Barnett, P Moscato, R Heard, R Scott Show all
Plos One | PUBLIC LIBRARY SCIENCE | Published : 2013
Abstract
Genome-wide association studies (GWAS) have identified around 60 common variants associated with multiple sclerosis (MS), but these loci only explain a fraction of the heritability of MS. Some missing heritability may be caused by rare variants that have been suggested to play an important role in the aetiology of complex diseases such as MS. However current genetic and statistical methods for detecting rare variants are expensive and time consuming. 'Population-based linkage analysis' (PBLA) or so called identity-by-descent (IBD) mapping is a novel way to detect rare variants in extant GWAS datasets. We employed BEAGLE fastIBD to search for rare MS variants utilising IBD mapping in a large ..
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Grants
Awarded by Australian Research Council
Funding Acknowledgements
This work was supported by the National Health and Medical Research Council (NHMRC, Australia) [Project 605511]; and the Australian Research Council [LP110100473]. MAB was supported by an NHMRC Senior Principal Research Fellowship. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.