Integrating mapping-, assembly- and haplotype-based approaches for calling variants in clinical sequencing applications

Andy Rimmer(University of Oxford), Hang Phan(Centre for Human Genetics), Iain Mathieson(University of Oxford), Zamin Iqbal(University of Oxford), Stephen R.F. Twigg(University of Oxford), Andrew O.M. Wilkie(John Radcliffe Hospital), Gil McVean(Centre for Human Genetics), Gerton Lunter(Centre for Human Genetics)
Nature Genetics
July 13, 2014
10.1038/ng.3036
Cited by 1,185Open Access
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