Copy number variation sequencing (CNV-seq) is a novel, high-throughput sequencing method to diagnose chromosomal aneuploides and microdeletions/microduplications as small as 0.1Mb from abortion tissues or blood samples, which could provide the genetic itiology for abortion or diseases, and also provide guidance for rebirth or treatment.
Annoroad CNV-seq adopts the next generation sequencing technology. Compared with G-band karyotype analysis, CNV-seq has a higher resolution for small CNVs and no need for cell culture.It also has other advantages, such as the ability to process a large number of samples simultaneously, diagnose with a high accuracy and precision rate, and discover more chromosomal abnormalities.
