Seed portfolio

PGTM-ChromSwift® Genetic Test for Monogenic Disease

Accurately detect the carrying status and block monogenic inherited diseases.

I am planning for pregnancy

Product Description

Product Benefits

Double verification

SNP linkage analysis and verification of pathogenic sites

Comprehensive & accurate

Simultaneous detection of chromosome aneuploidy

Mature platform

Valuable detection data of tens of thousands of embryos and hundreds of monogenic diseases

Exclusive insurance

Comprehensive protection, no worries

For Who

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

Service Process