BioDiscovery Resources
BioDiscovery Webinars
Watch informative webinars and demonstrations from industry leaders.
See how our products have been used to aid in the clinical and research fields, and to help detect cancer.
Choose by Resource, then filter by Product OR Topic
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.
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.
Real-world experience utilizing NxClinical for CNV detection using standard-of-care testing in Post-natal specimens
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Implementing high-throughput cloud-based microarray analysis in the UK Genomic Medicine service
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Embracing the power of the SNP. NxClinical facilitates detection of UPD and determination of parent of origin from SNP microarray data.
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
Significance Associated with Phenotype (SAP) Score: A Method for Ranking Genes and Genomic Regions Based on Patient’s Phenotype
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
An unorthodox journey and our experience for validation of NxClinical and the GSA Beadchip microarray
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
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.
A retrospective evaluation of 211 clinical referrals for intellectual disability testing
This webinar is geared towards those involved with genomic variation analysis and interpretation in a cytogenetics or molecular genetics lab.
