Fig. 2From: mGAP: the macaque genotype and phenotype resource, a framework for accessing and interpreting macaque variant data, and identifying new models of human diseaseVariant annotation strategy. Macaque variant data are first lifted to the human genome (GRCh37), and annotated against multiple sources. The resulting variants are translated back to the original rhesus macaque coordinates (MMul8.0.1), and merged with the non-lifted variantsBack to article page