Genetic Compass for Healthy Generations
PGT-SR enables the detection of aneuploid embryos resulting from structural chromosomal rearrangements, such as translocations and insertions. In cases with a family history of chromosomal translocations, recurrent pregnancy loss associated with structural chromosomal abnormalities, or known structural rearrangement carrier status, chromosomal imbalances beyond the scope of PGT-A can be evaluated using PGT-SR. This helps reduce the risk of adverse pregnancy outcomes associated with structural chromosomal abnormalities by enabling the selection of chromosomally balanced embryos for transfer.
Conditions Screened by PGT-SR:
Technical Specifications
Feature | Details |
Method | NGS (Next-Generation Sequencing) + Fragment Analysis |
Coverage | All chromosomes (24 Chromosomes) |
Sample Requirement | Day 5 biopsy (trophectoderm) |
Turnaround Time (TAT) | Approximately 7-14 days |
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