BioDiscovery Webinars

Topic: Rare Disease

Rapid implementation of the latest technical standards with the NxClinical integrated ACMG scoreboard

This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from microarray data in cytogenetics or molecular genetics labs.

Copy Number Variant Detection by NGS: Coverage, Uniformity & Resolution

This webinar is geared towards those involved with genomic variation analysis and interpretation of copy number variation (CNV) from next-generation sequencing (NGS) data in cytogenetics or molecular genetics labs.

Genome sequencing reveals cause of multi-generational split hand/split foot with long bone deficiency

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