Reproductive Genetics-Professional Edition-details

Product Description

PGT-M detects the carrying status of the pathogenic mutation of the monogenic inherited disease and the chromosome abnormality above 4M, so as to screen the embryo to transfer that do not carry the pathogenic gene mutation and the chromosomal abnormality.

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

PGTM-ChromSwift^® Genetic Test for Monogenic Disease

Product Description

Product Benefits

For Who

Service Process

Our Services

Carrier Screening for Monogenic Inherited Diseases (442 diseases, CSKB)

Carrier Screening of Monogenic Inherited Diseases (20 diseases, CSKA)

PGTSR-ChromInst^® Preimplantation Genetic Testing for Chromosomal Structural Arrangement (PGT-SR)

PGTA-ChromInst^® Molecular Genetic Test for Aneuploidy (PGT-A)