BGI is the first batch of high-throughput gene sequencing technology application pilots for genetic diseases, preimplantation embryo genetic diagnosis and tumor diagnosis and ** project of the National Health Commission, and is a high-quality examination institution dedicated to scientific and technological innovation and reducing birth defects.
In order for more and more pregnant mothers to enjoy the convenience and safety of prenatal screening, BGI has released a series of non-invasive prenatal genetic testing, among which the NIFTY all-cause series subverts everyone's perception of the original prenatal screening, which does not need to pass the efficient but damaging amniocentesis or inefficient but safe Down's screening, and can also allow pregnant mothers to gain the best of both worlds with a high detection rate and no risk of miscarriage. The inspection location may not be available in the mainland, there is a wide range of locations in Hong Kong, and you can experience the car reception service by making an appointment at the Central Specialist in Hong Kong**.
The NIFTY series has the original basic version and the PRO upgraded version, and the innovative technology PRO can comprehensively and accurately screen for fetal chromosomal abnormalities. What diseases does BGI NIFTY test for? It covers a wide range of tests, including 6 trisomy syndromes, 4 sex chromosome abnormalities, and 84 definite chromosomal deletion duplication syndromes. By increasing the amount of data to 25m, which ensures high accuracy, the introduction of this technology will undoubtedly provide accurate and effective support for clinical diagnosis and **.
What diseases does BGI NIFTY test for? In addition to detecting the common trisomy down, Nifty Pro is also effective in identifying sex chromosomal abnormalities. In addition, the detection range also covers other autosomal aneuploidy abnormalities such as trisomy 16 and trisomy 22. At the same time, the simultaneous detection of 84 chromosomal deletion duplication syndromes with clear clinical significance and severe clinical manifestations is a high-quality non-invasive examination with complete performance for pregnant mothers who want to know the comprehensive chromosomal health of the fetus!