@misc{indiciae680b69bd25bf,
  title = {A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies},
  author = {Li, X. and Chen, H. and Selvaraj, M. S. and Van Buren, E. and Zhou, H. and Wang, Y. and Sun, R. and McCaw, Z. R. and Yu, Z. and Arnett, D. K. and Bis, J. C. and Blangero, J. and Boerwinkle, E. and Bowden, D. W. and Brody, J. A. and Cade, B. E. and Carson, A. P. and Carlson, J. C. and Chami, N. and Chen, Y.-D. I. and Curran, J. E. and de Vries, P. S. and Fornage, M. and Franceschini, N. and Freedman, B. I. and Gu, C. and Heard-Costa, N. L. and He, J. and Hou, L. and Hung, Y.-J. and Irvin, M. R. and Kaplan, R. C. and Kardia, S. L. R. and Kelly, T. and Konigsberg, I. and Kooperberg, C. and Kral, B. G. and Li, C. and Loos, R. J. F. and Mahaney, M. C. and Martin, L. W. and Mathias, R. A. and Minster, R. L. and Mitchell, B. D},
  year = {2023},
  doi = {10.1101/2023.10.30.564764},
  url = {https://www.biorxiv.org/content/10.1101/2023.10.30.564764v1},
  note = {Source identifier: 10.1101/2023.10.30.564764}
}