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Original article
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
- Correspondence to Dr Alexander E Urban, Department of Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Stanford, CA 94305, USA; aeurban{at}stanford.edu
Citation
Whole-genome sequencing analysis of CNV using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis
Publication history
- Received January 18, 2018
- Revised May 16, 2018
- Accepted June 26, 2018
- First published July 30, 2018.
Online issue publication
October 26, 2018
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© Author(s) (or their employer(s)) 2018. No commercial re-use. See rights and permissions. Published by BMJ.