
EmbryoMap™
NGS-based PGT-A kit using whole genome amplification and next-generation sequencing. Detects trisomy, monosomy, and structural abnormalities across all 24 chromosomes.
Key features
- PGT-A aneuploidy screening
- NGS-based platform
- Whole genome amplification
- All 24 chromosomes
- Structural variants detected
- Single-tube workflow
