Identification of copy number variants by NGS-based NIPT at low sequencing depth
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Title
Identification of copy number variants by NGS-based NIPT at low sequencing depth
Authors
Keywords
Noninvasive prenatal testing, Copy number variants, lOw-Pass whole-genome sequencing, Chromosomal microarray analysis, Sensitivity, Specificity
Journal
European Journal of Obstetrics & Gynecology and Reproductive Biology
Volume 256, Issue -, Pages 297-301
Publisher
Elsevier BV
Online
2020-11-12
DOI
10.1016/j.ejogrb.2020.11.026
References
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Related references
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