@misc{indiciae063971f08c1e,
  title = {Identification of Pathogenic Structural Variants in Rare Disease Patients through Genome Sequencing},
  author = {Holt, J. M. and Birch, C. L. and Brown, D. M. and Gajapathy, M. and Sosonkina, N. and Wilk, B. and Wilk, M. and Spillmann, R. C. and Stong, N. and Lee, H. and Huang, A. Y. and Bonner, D. and Kohler, J. N. and Macnamara, E. F. and Diseases Network, U. and Nelson, S. F. and Shashi, V. and Worthey, E. A.},
  year = {2019},
  doi = {10.1101/627661},
  url = {https://www.biorxiv.org/content/10.1101/627661v1},
  note = {Source identifier: 10.1101/627661}
}