BioDiscovery Webinars

Topic: Whole Exome Sequencing

Demonstrating How You Can Obtain More Answers from Your NGS Data by Using Bionano's NxClinical Software

This webinar is geared toward those involved with genomic variation analysis and interpretation of Copy Number Variation from next-generation sequencing (NGS) data in cytogenetics, molecular pathology, or molecular genetics labs.

Increasing the yield of whole exome sequencing (WES) with CNV analysis

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