Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
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Title
Low‐pass whole genome sequencing is a reliable and cost‐effective approach for copy number variant analysis in the clinical setting
Authors
Keywords
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Journal
ANNALS OF HUMAN GENETICS
Volume -, Issue -, Pages -
Publisher
Wiley
Online
2023-10-12
DOI
10.1111/ahg.12532
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