Analysis of copy number variants detected by sequencing in spontaneous abortion.

Anhui LiuLiyuan ZhouYazhou HuangDan Peng

Published in: Molecular cytogenetics (2024)

CNV sequencing (CNV-seq) analysis is an effective technique for detecting chromosomal abnormalities in POCs and identifying potential candidate genes for SA.

Keyphrases

copy number
mitochondrial dna
genome wide
single cell
dna methylation
rna seq
gene expression
risk assessment
human health
climate change
data analysis