@misc{indiciae6abfd89472c7,
  title = {Identification and prioritisation of causal variants in human genetic disorders from exome or whole genome sequencing data},
  author = {Paramasivam, N. and Granzow, M. and Evers, C. and Hinderhofer, K. and Wiemann, S. and Bartram, C. R. and Eils, R. and Schlesner, M.},
  year = {2017},
  doi = {10.1101/209882},
  url = {https://www.biorxiv.org/content/10.1101/209882v1},
  note = {Source identifier: 10.1101/209882}
}