@misc{indiciae67becaef2df8,
  title = {Software-assisted manual review of clinical NGS data:an alternative to routine Sanger sequencing confirmationwith equivalent results in >15,000 hereditary cancer screens},
  author = {Muzzey, D. and Kash, S. and Johnson, J. I. and Melroy, L. M. and Kaleta, P. and Pierce, K. A. and Ready, K. and Kang, H. P. and Haas, K. R.},
  year = {2018},
  doi = {10.1101/305011},
  url = {https://www.biorxiv.org/content/10.1101/305011v1},
  note = {Source identifier: 10.1101/305011}
}