TY  - RPRT
TI  - 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
AU  - Zhou, B.
AU  - Ho, S. S.
AU  - Zhang, X.
AU  - Pattni, R.
AU  - Haraksingh, R. R.
AU  - Urban, A. E.
PY  - 2017
DO  - 10.1101/192310
UR  - https://www.biorxiv.org/content/10.1101/192310v1
ID  - 10.1101/192310
ER  -