Lineagen, a Bionano Genomics Company has utilized the N_xClinical software for the interpretation of copy number variations (CNVs) in post-natal populations. Join us as we describe our experience in utilizing this platform-agnostic software to merge databases from multiple clinically available platforms for improved clinical workflow. Two of Lineagen’s lab directors will describe their real-world experience of utilizing the variant database, pre-classification, custom tracks, and other functionalities while highlighting a few case examples.

 

Audience:

This webinar is geared towards those involved with genomic variation analysis and interpretation of microarray data in a cytogenetics or molecular genetics lab.