Description
PGT-A (formerly known as PGS) is a genetic test performed on embryos to detect numerical chromosomal abnormalities (aneuploidy). Our PGT-A utilizes Next-Generation Sequencing (NGS) to analyze all 24 chromosomes, ensuring chromosomal abnormalities are identified before embryo transfer. This enables informed decisions and increases the chances of a successful pregnancy.
Test code(s)
BNG-560, BNG-574
TAT
5 business days
Method
NGS (Next-Generation Sequencing), low pass whole genome
Accepted Sample requirements
single cell biopsy on day 3 of development and trophectoderm biopsy.