@misc{indiciae1fdb83f9a3e4,
  title = {Low coverage whole genome sequencing enables accurate assessment of common variants and calculation of genome-wide polygenic scores},
  author = {Homburger, J. R. and Neben, C. L. and Mishne, G. and Zhou, A. Y. and Kathiresan, S. and Khera, A. V.},
  year = {2019},
  doi = {10.1101/716977},
  url = {https://www.biorxiv.org/content/10.1101/716977v1},
  note = {Source identifier: 10.1101/716977}
}