A Rapid PCR-Free Next-Generation Sequencing Method for the Detection of Copy Number Variations in Prenatal Samples

Next-generation sequencing (NGS) is emerging as a new method for the detection of clinically significant copy number variants (CNVs). In this study, we developed and validated rapid CNV-sequencing (rCNV-seq) for clinical application in prenatal diagnosis. Low-pass whole-genome sequencing was perform...

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Detalhes bibliográficos
Publicado no:Life (Basel)
Main Authors: Zhou, Xiya, Chen, Xiangbin, Jiang, Yulin, Qi, Qingwei, Hao, Na, Liu, Chengkun, Xu, Mengnan, Cram, David S., Liu, Juntao
Formato: Artigo
Idioma:Inglês
Publicado em: MDPI 2021
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7911416/
https://ncbi.nlm.nih.gov/pubmed/33525582
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/life11020098
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