Hereditary NGS Clinical Summit Series: Build a Next-Gen Software Workflow for Germline Testing

Over the past two decades, huge advancements in sequencing technology have transformed our understanding of human genetics, leading to faster diagnoses, earlier prevention, and better treatments. But as more and more people have their genomes sequenced, outpacing our ability to analyze and interpret the generated data, we must embrace new tools, technologies, and strategies to realize the full value of genomic innovation.

Advance your lab’s germline testing capabilities by learning how to build a next-gen software workflow, as part of the Hereditary NGS Clinical Summit Series, a two-part, free-to-attend virtual event for variant scientists, bioinformaticians, clinical geneticists, and lab managers.  

Part I: Thursday, October 13, 2022 

An informative scientific and clinical segment focusing on how to streamline and scale components of the NGS analytical workflow.

Attendees will learn:

• How to simplify NGS secondary analysis workflows to 5 steps
• How to solve every hereditary disorder case for all types of mutations
• How to address current challenges in germline and exome analytics