Male infertility remains a complex and underdiagnosed condition, with many genetic causes that are not captured by conventional diagnostic methods like karyotyping or Y-chromosome microdeletion analysis.
In this webinar, Dr. Harsh Sheth delves into how next-generation sequencing (NGS) is enabling more comprehensive and accurate genetic evaluation. The discussion focuses on the role of monogenic causes in infertility and how advanced molecular techniques, particularly the use of single-molecule molecular inversion probes (smMIPs), are improving variant detection with high precision and cost-efficiency. Alongside the technical aspects of assay design and validation, the session provides practical guidance on integrating NGS assays into clinical workflows, helping labs and clinicians enhance diagnostic yield and make genomic testing more accessible for patients.
If you’re working on reproductive health diagnostics or genomics-driven solutions, this session is packed with technical depth and actionable ideas.
