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Whole-genome sequencing analysis of copy number variation (CNV) using low-coverage and paired-end strategies is efficient and outperforms array-based CNV analysis

Published in 2017 by Bo Zhou ORCID, Steve S. Ho ORCID, Xianglong Zhang ORCID, Reenal Pattni ORCID, Rajini R. Haraksingh ORCID, Alexander E. Urban ORCID
This paper was not found in any repository; the policy of its publisher is unknown or unclear.
This paper was not found in any repository; the policy of its publisher is unknown or unclear.

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