First NIPT test
Quickly and early detection of the most common and dangerous birth defects for the fetus
Exactly
Safe
Convenient
Cost optimization
NextGen - future generation
Genetic testing is a gift for a brighter future, and NextGen's mission is to use the most advanced genetic technology to ensure a better future.
- A team of professional doctors and engineers in Taiwan
- Spend a long time continuously improving technical technology
- Professional, safe, accurate and convenient non-invasive testing
- Use technology to prevent and predict potential health risks
Advantages at NextGen
Modern technology, meeting international standards
The entire blood sample analysis process is performed at a US CAP standard laboratory.
A team of experienced experts
The team of professional doctors and engineers in Taiwan has spent a long time making continuous improvements in technical technology.
Granted a patent
The entire blood sample analysis process is performed at a laboratory that meets CAP standards in the United States and Taiwan.
Fast result return time
NIPT test results at NextGEN are returned as soon as 5-10 days of implementation.
NextGen ecosystem
Genetic testing of mother and baby
The laboratory is CAP certified in the United States and test results are according to international standards.
See details
Test package to assess disease risk
Fragile X Syndrome, FXS; Spinal muscular atrophy, SMA; Huntington, HD
See details
Disease risk testing
Alzheimer's disease (dementia); hemophilia; Hereditary stroke (CADASIL); Parkinson disease,...
See details
NIPT testing procedure
The NIPT testing process must ensure strictness, no sample confusion, sample contamination, and each step must be performed correctly.
1
Consulting on NIPT testing methods
Doctors examine and advise in detail about NIPT testing to help pregnant mothers understand the benefits of prenatal screening for the fetus. From there, mothers choose the appropriate and necessary screening package.
2
Take a sample of the mother's blood
Doctors examine and advise in detail about NIPT testing to help pregnant mothers understand the benefits of prenatal screening for the fetus. From there, mothers choose the appropriate and necessary screening package.
3
Gene sequencing with Next Generation technology
Doctors examine and advise in detail about NIPT testing to help pregnant mothers understand the benefits of prenatal screening for the fetus. From there, mothers choose the appropriate and necessary screening package.
4
Analyze data from Fetal Genomics
Doctors examine and advise in detail about NIPT testing to help pregnant mothers understand the benefits of prenatal screening for the fetus. From there, mothers choose the appropriate and necessary screening package.
5
Report results to obstetrician and explain and advise
Doctors examine and advise in detail about NIPT testing to help pregnant mothers understand the benefits of prenatal screening for the fetus. From there, mothers choose the appropriate and necessary screening package.
Service package at NextGen
- Down syndrome (Trisomy 21)
- Edward Syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Turner syndrome (Turner syndromeXO)
- Klinefelter syndrome (Klinefelter syndrome XXY)
Support for amniocentesis test fees when there are abnormal NIPT results
- Down syndrome (Trisomy 21)
- Edward Syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Turner syndrome (Turner syndromeXO)
- Klinefelter syndrome(Klinefelter syndrome XXY)
1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 19, 20, 22, triploid.
- Down syndrome (Trisomy 21)
- Edward Syndrome (Trisomy 18)
- Patau syndrome (Trisomy 13)
- Turner syndrome (Turner syndromeXO)
- Klinefelter syndrome (Klinefelter syndrome XXY)
1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 14, 15, 16, 17, 19, 20, 22, triploid.
- 1p36 deletion syndrome
- DiGeorge syndrome
- Wolf-Hirschhorn Syndrome
- Cri du chat syndrome (Meowing cat syndrome)
- Smith Maggie Syndrome
- Williams-Beuren syndrome
- 22q|2 deletion syndrome
- 1p36 deletion syndrome
- DiCeorge syndrome
- Wolf-Hirschhorn Syndrome
- Cri du chat syndrome (Meowing cat syndrome)
- Smith-Maggie Syndrome
- Williams-Beuren syndrome
- 22q11.2 long deletion syndrome
- NHI small fragment deletion mutation
- Prader-Willi syndrome
- Angelman syndrome
- Sotos syndrome
- Kolen de vries congregation
- ATR16 syndrome
- Potocki-Shaffer syndrome
- Miller-Dieker Syndrome
- Glass Syndrome
Featured news
The NIPT testing process must ensure strictness, no sample confusion, sample contamination, and each step must be performed correctly.
Find out more
INTERNATIONAL CONFERENCE PROGRAM ON PRE-BIRTH GENETIC TESTING IN 2023
Application of New Technology in Medical Equipment
Application of New Technology in Medical Equipment
Distinguishing Types of High Quality Medical Equipment
The Importance of Medical Supplies Products in Hospital Management
NextGen Partner
The NIPT testing process must ensure strictness, no sample confusion, sample contamination, and each step must be performed correctly.
Sign up for consultation
