Using High-Resolution Variant Frequencies Empowers Clinical Genome Interpretation and Enables Investigation of

Nicola Whiffin1, Angharad M Roberts2, Eric Minikel3

  • 1Cardiovascular Genetics and Genomics, National Heart and Lung Institute, Imperial College Centre for Translational and Experimental Medicine, London, W12 0NN, UK; National Institute for Health Research Royal Brompton Cardiovascular Research Centre, Royal Brompton and Harefield National Health Service Foundation Trust, London, SW7 2AZ, UK; Medical Research Council London Institute of Medical Sciences, Imperial College London, London, W12 0NN, UK.

Abstract

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