With PGD-seq, the PGT-M (PGD) and PGT-A (PGS) tests can be combined to study chromosomal aneuploidies, monogenic diseases and to copy the number variations, starting from a single biopsy. The study could be applied in the same sequencing run.

In addition, multiple samples can be processed together in such a way that the sequencing time and cost per sample are minimized.