NGS, or Next Generation Sequencing, is an advanced genetic diagnostic test that allows a detailed examination of all 46 chromosomes in embryos. Unlike older methods, NGS provides a more comprehensive and precise analysis, helping identify chromosomal problems before pregnancy begins.
One of the leading reasons why healthy pregnancies may fail to occur despite successful embryo transfers is the presence of chromosomal abnormalities.
Who Can Benefit from NGS?
NGS is particularly recommended for:
Women over 38 years of age
Couples with recurrent pregnancy loss
Couples with multiple failed IVF attempts
Cases where chromosomal issues (such as deletions or duplications) are detected in either parent
How the Process Works
On the day of egg retrieval or ICSI, sperm cells are injected into the eggs using the microinjection technique.
The resulting embryos are monitored in the laboratory for 5–6 days until they reach the blastocyst stage.
A small biopsy of 5–6 cells is taken from the trophectoderm (outer cell layer), while leaving the inner cell mass untouched.
The sampled embryos are frozen the same day, and the NGS screening process takes about 2–3 weeks.
Once results are ready, the mother begins preparation for transfer. The healthiest embryos are then selected and transferred into the uterus.
Any remaining healthy embryos are safely frozen for future use.
Why Choose Us?
At Cyprus American IVF Center, NGS is performed entirely in-house using our state-of-the-art NGS device. Our experienced embryologists and genetics team ensure the highest level of accuracy without sending samples to external laboratories.
This advanced approach helps increase the chances of a healthy pregnancy while reducing risks associated with genetic abnormalities.
Stay Healthy,
Cyprus American IVF Center
