Accurately detect the carrying status and block monogenic inherited diseases.
SNP linkage analysis and verification of pathogenic sites
Simultaneous detection of chromosome aneuploidy
Valuable detection data of tens of thousands of embryos and hundreds of monogenic diseases
Comprehensive protection, no worries
1 Monogenic inherited disease: couples carrying high risk of having offspring with single-gene inherited diseases, or clearly diagnosed of the disease-causing gene mutation.
2 Serious diseases with genetic susceptibility: such as the BRCA1/BRCA2 pathogenic mutations of inherited breast cancer
3 Human Leukocyte Antigen (HLA) Matching
Aimed to provides more comprehensive primary prevention and control of birth defects Carrier Screening-Plus has covered 442 monogenic diseases in 13 major clinical diagnostics fields through broadening testing scope
In the ultra-non-invasive age, Carrier Screening is to lead the high-level prevention and control of birth defects
Comprehensive detection of embryo chromosomal abnormality, and effectively solve the problem of recurrent miscarriage in patients with abnormal chromosome structure