@misc{indiciae7b408c2e61b5,
  title = {De novo assembly of two Swedish genomes reveals missing segments from the human GRCh38 reference and improves variant calling of population-scale sequencing data},
  author = {Ameur, A. and Che, H. and Martin, M. and Bunikis, I. and Dahlberg, J. and Höijer, I. and Häggqvist, S. and Vezzi, F. and Nordlund, J. and Olason, P. and Feuk, L. and Gyllensten, U.},
  year = {2018},
  doi = {10.1101/267062},
  url = {https://www.biorxiv.org/content/10.1101/267062v1},
  note = {Source identifier: 10.1101/267062}
}