@misc{indiciae517f6c5e391d,
  title = {Matching whole genomes to rare genetic disorders: Identification of potential causative variants using phenotype-weighted knowledge in the CAGI SickKids5 clinical genomes challenge},
  author = {Pal, L. R. and Kundu, K. and Yin, Y. and Moult, J.},
  year = {2019},
  doi = {10.1101/707687},
  url = {https://www.biorxiv.org/content/10.1101/707687v1},
  note = {Source identifier: 10.1101/707687}
}