Everything you need for Business



Prenatal Service for Maternal Hospitals

Next Generation DNA Test, 100% safe for mother and child with 0% risk of miscarriage. Fast and accurate non-invasive screen for the most common fetal abnormalities related to chromosomes 13, 18, 21, X/Y, and more.

After 10 weeks of pregnancy, NIPT can detect whether your baby is at risk of Trisomy13, 18, 21, Sex chromosome aneuploidies and Gender information within less than 7 days, need only 10ml of maternal blood.


We are looking for a partner who want to take our technology or distributing this NIPT service to your local site.



Embryo Genetic Screening for IVF centers

GenoBro is an NGS-based PGS(pre-implantation screening) test that selects genetically normal embryos. It has a much higher sensitivity and suspend time than conventional methods (FISH, aCGH) and can shorten inspection time as shorten as 24 hours.

Unlike other lab facility we offer better shipping condition, 

so you can send us prepped DNA instead of frozen embryo.

If you are interested in PGS, let’s start from sampling test.


Newborn Screening

Inborn disorders identifying for newborn baby

Newborn screening intends to identify inborn disorders that can result in early mortality or lifelong disability.

The NewbornDiscovery is a NGS-based clinical genomic analytic that can identify over 100 diseases from newborns’ dried blood spots or blood. Currently we offer NGS-based clinical genomic analytic service which includes gene panel analyzing 108 genes (Focused) / 350 genes (Extended) for newborn screening.


If you interested in Newborn Screening, please contact us  info@genomecare.net