Experience of copy number variation sequencing applied in spontaneous abortion

Experience of copy number variation sequencing applied in spontaneous abortion

Abstract Purpose We evaluated the value of copy number variation sequencing (CNV-seq) and quantitative fluorescence (QF)-PCR for analyzing chromosomal abnormalities (CA) in spontaneous abortion specimens. Methods A total of 650 products of conception (POCs) were collected from spontaneous abortion b...

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Bibliographic Details
Main Authors: Yi-Fang Dai, Xiao-Qing Wu, Hai-Long Huang, Shu-Qiong He, Dan-Hua Guo, Ying Li, Na Lin, Liang-Pu Xu
Format: Article
Language:English
Published: BMC 2024-01-01
Series:BMC Medical Genomics
Subjects:
High-throughput nucleotide sequencing
Genetics
Chromosome aberrations
Online Access:https://doi.org/10.1186/s12920-023-01699-1
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https://doi.org/10.1186/s12920-023-01699-1

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