Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting https://www.medrxiv.org/content/10.1101/2023.05.26.23290606
Low-pass whole genome sequencing is a reliable and cost-effective approach for copy number variant analysis in the clinical setting https://www.medrxiv.org/content/10.1101/2023.05.26.23290606