BioDiscovery Webinars

Topic: Next Gen 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.

Next-Generation Sequencing Assessment of HRD

This webinar is geared towards those involved with genomic variation analysis and interpretation of homologous recombination deficiency (HRD) from microarray data or next-generation sequencing (NGS) data in cytogenetics, molecular pathology, 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.