@misc{indiciae7c6693b0729e,
  title = {Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease},
  author = {Merker, J. and Wenger, A. M. and Sneddon, T. and Grove, M. and Waggott, D. and Utiramerur, S. and Hou, Y. and Lambert, C. C. and Eng, K. S. and Hickey, L. and Korlach, J. and Ford, J. and Ashley, E. A.},
  year = {2016},
  doi = {10.1101/090985},
  url = {https://www.biorxiv.org/content/10.1101/090985v1},
  note = {Source identifier: 10.1101/090985}
}