Gil McVean

The variant call format and VCFtools

Petr Danecek, Adam Auton, Gonçalo R. Abecasis et al. · Bioinformatics · 2011 · 16.8K citations · Full text

The UK Biobank resource with deep phenotyping and genomic data

Clare Bycroft, Colin Freeman, Desislava Petkova et al. · Nature · 2018 · 9.2K citations · Full text

Detecting Novel Associations in Large Data Sets

David N. Reshef, Yakir Reshef, Hilary K. Finucane et al. · Science · 2011 · 3.3K citations

A new multipoint method for genome-wide association studies by imputation of genotypes

Jonathan Marchini, Bryan Howie, Simon Myers et al. · Nature Genetics · 2007 · 2.7K citations

Genome-wide Association Study, Genetic Analysis, Haplotype Determination +13

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

Andy Rimmer, Hang Phan, Iain Mathieson et al. · Nature Genetics · 2014 · 1.2K citations · Full text

Long-read Sequencing, Haplotype Determination, Allelic Variant +14