Login / Signup

Prenatal diagnosis of 913 fetuses samples using copy number variation sequencing.

Liubing LanLingna SheBosen ZhangYanhong HeZhiyuan Zheng
Published in: The journal of gene medicine (2021)
Compared with karyotype analysis, CNV-seq can improve the detection rate of chromosomal abnormalities. CNV-seq combined karyotype analysis should be performed simultaneously in fetuses with puncture indications.
Keyphrases
  • copy number
  • genome wide
  • mitochondrial dna
  • single cell
  • dna methylation
  • gestational age
  • label free
  • sensitive detection