In this webinar MGI introduced both PGS (Preimplantation Genetic Screening) for detecting embryonic chromosomal CNVs and PGD (Preimplantation Genetic Diagnosis) for inherited monogenic diseases with haplotype phasing. The integration and customization of these two tests as an one-stop solution was showcased, including: sample preparation, library preparation, sequencing, data analysis, and reporting. With optimized protocols, automation, and analysis pipelines, all as part of MGI's PGS Total Solution which allows users to easily go from sample to report.