@misc{indiciae6c34b09dcf9b,
  title = {A survey of rare epigenetic variation in 23,116 human genomes identifies disease-relevant epivariations and novel CGG expansions},
  author = {Garg, P. and Jadhav, B. and Rodriguez, O. J. and Patel, N. and Martin-Trujillo, A. and Jain, M. and Metsu, S. and Olsen, H. and Paten, B. and Ritz, B. and Kooy, F. and Gecz, J. and Sharp, A. J.},
  year = {2020},
  doi = {10.1101/2020.03.25.007864},
  url = {https://www.biorxiv.org/content/10.1101/2020.03.25.007864v1},
  note = {Source identifier: 10.1101/2020.03.25.007864}
}