Fig. 1
From: Characterisation of pharmacogenomic variation in the Shetland and Orkney Isles in Scotland
Overview of the study design and outline. Viking Genes is a project including cross-sectional studies aiming to identify genetic factors influencing complex disease risk in the population isolates of the Shetland and Orkney Isles in northern Scotland. Binary Alignment Map (BAM) files and Variant Call Format (VCF) files used in this study have been generated in previous studies in Viking Genes14 and by the New York Genome Center (for the 1000 Genomes datasets)20. SV: Structural Variant, VEP: Variant Effect Predictor, CPIC: Clinical Pharmacogenetics Implementation Consortium.
