Abstract

Preimplantation genetic screening (PGS) wants to improve artificial reproductive technologies (ART), primarily by raising the rates of pregnancy, implantation and birth. At the moment there are two main approaches for PGS: biopsy of blastocysts, predominantly in the USA, and polar body biopsy, in Europe, both now combined with array comparative genome hybridization (aCGH). Improvement was contested for a long time. And aCGH is expensive when applied to the many oocytes per cycle in comparison to the few blastocysts per cycle.

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