BioDiscovery Webinars

Topic: Whole Genome Sequencing

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.