To stay ahead in the ever so rapidly evolving field of genomics, molecular labs need software that can keep up with the pace. As test menus expand, nomenclature changes, new assays arrive, and the reporting expectations of treating clinicians keep rising, a laboratory that runs production diagnostics needs an IT solution that moves at the same speed.
In this webinar, Sectra & Penn Medicine demonstrate how a lab work and interpretation come together in a integrated genomics solution by following a case from order entry to final report, and discuss what it takes to keep a clinical system current as the field moves.
Learning Objectives
After viewing this webinar, you will be able to:
- How an end-to-end genomics workflow fits together, from order receipt to structured results in the EMR
- How wet lab operations, sequencing quality control and variant interpretation work in a single application with one audit trail
- How built-in quality controls, hard stops and contamination checks support a laboratory working under CAP and CLIA accreditation
- How a laboratory adds new assays, classification schemes and reporting requirements without a vendor project each time
- How to future-proof your genomics journey
This webinar was recorded on the AMP Annual Meeting Nov 11, 2025
Speakers

Fredrik Lysholm, PhD
General Manager, Genomics IT
Sectra

Salvatore F. Priore, MD, PhD
Associate Director, Division of Precision and Computational Diagnostics
Penn Medicine

