Next generation sequencing (NGS) technology has been used in embryos since late 2014 for genetic diagnosis (PGD).
Using NGS technique, 24 chromosome examinations in embryos have some advantages over other methods. In particular, it has been reported that mosaic embryos are more likely to be identified by this method. In addition, BAC or oligo based probes are used in the array CGH methods used in the probes due to a number of problems are much less observed.
Please click here to access the iti NGS PGS Brochure adı which was prepared with the VeriSeq kit developed by Illumina and shared with you with the important information about this method called NGS PGS.