@misc{indiciae57cbcc7d13fc,
  title = {Targeted long-read sequencing resolves complex structural variants and identifies missing disease-causing variants},
  author = {Miller, D. E. and Sulovari, A. and Wang, T. and Loucks, H. and Hoekzema, K. and Munson, K. M. and Lewis, A. P. and Almanza Fuerte, E. P. and Paschal, C. R. and Thies, J. and Bennett, J. T. and Glass, I. and Dipple, K. M. and Patterson, K. and Bonkowski, E. S. and Nelson, Z. and Squire, A. and Sikes, M. and Beckman, E. and Bennett, R. L. and Earl, D. and Lee, W. and Allikmets, R. and Perlman, S. J. and Chow, P. and Hing, A. V. and Adam, M. P. and Sun, A. and Lam, C. and Chang, I. and University of Washington Center for Mendelian Genomics, and Cherry, T. and Chong, J. X. and Bamshad, M. J. and Nickerson, D. A. and Mefford, H. C. and Doherty, D. and Eichler, E. E.},
  year = {2020},
  doi = {10.1101/2020.11.03.365395},
  url = {https://www.biorxiv.org/content/10.1101/2020.11.03.365395v1},
  note = {Source identifier: 10.1101/2020.11.03.365395}
}