@misc{indiciaeea680f62cff0,
  title = {Response to Shah et al: Using high-resolution variant frequencies empowers clinical genome interpretation and enables investigation of genetic architecture},
  author = {Whiffin, N. and Roberts, A. and Minikel, E. V. and Zappala, Z. and Walsh, R. and O'Donnell-Luria, A. H. and Karczewski, K. and Harrison, S. M. and Thomson, K. L. and Sage, H. and Ing, A. Y. and Barton, P. J. R. and Cook, S. A. and MacArthur, D. G. and Ware, J. S.},
  year = {2018},
  doi = {10.1101/384271},
  url = {https://www.biorxiv.org/content/10.1101/384271v1},
  note = {Source identifier: 10.1101/384271}
}