1.Introduction to genetics and medical genomics

2.Meiosis, oogenesis and spermatogenesis

3.Post-fertilization mitotic divisions and embryonic mosaicism

4.Embryo biopsy: update

5.PGT for monogenic disorders and carrier screening

6.PGT for chromosome abnormalities and chromosome rearrangements

7.The PGT-A controversy

8.Future directions for the molecular assessment and diagnosis of embryos

9.Genetic Counseling in the infertile/sterile couple

10.Reproductive genomics: basic concepts, consortia, databases and genome datasets

11.Techniques for genomic analysis: preliminary, exploratory and functional

12.Techniques for systems genomic analysis: network modelling

13.Genomic tools for computational prediction and clinical application

14.Genetic Diagnosis of the Endometrial Factor: controversies

15.Analysis of genome variants: prioritization of clinical biomarkers and gene panels in the diagnosis

16.Systems Reproduction Medicine: the big data era