@misc{indiciaee50368542a88,
  title = {Whole-genome sequencing analysis of genomic copy number variation (CNV) using low-coverage and paired-end strategies is highly efficient and outperforms array based CNV analysis},
  author = {Zhou, B. and Ho, S. S. and Zhang, X. and Pattni, R. and Haraksingh, R. R. and Urban, A. E.},
  year = {2017},
  doi = {10.1101/192310},
  url = {https://www.biorxiv.org/content/10.1101/192310v1},
  note = {Source identifier: 10.1101/192310}
}