BioDiscovery Webinars

Topic: Ngs

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.

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.

Integrated analysis of SNVs, CNVs, and AOH facilitates accurate diagnosis in Mendelian disorders & pediatric cancers

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

Increased diagnostic accuracy for Mendelian disorders and pediatric cancers through integrated review of SNVs, CNVs and regions of homozygosity

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

Combined Analysis and Interpretation of CNV, AOH, and Seq Var of FFPE Cancer Samples from a Solid Tumor NGS Panel

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

Challenges and Solutions to Copy Number Estimation from Whole Exome Sequencing in Tumors

This webinar is geared towards those requiring copy number results from low coverage sequencing results (shallow/targeted) and/or from normal coverage WGS/WES results.