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.

Highlights of NxClinical 4.1: Improved Sequence Variant Interpretation and Support for the Newest Array Platforms Recording

Dr. Soheil Shams discusses the highlights of NxClinical 4.1: Improved Sequence Variant Interpretation and Support for the Newest Array Platforms Recording

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

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

NxClinical 4.0 – CNV, SeqVar, and AOH from a single NGS assay

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

Downstream Research Analysis of Copy Number from NGS in Cancer Samples

This webinar is geared towards those working on research projects and want to know what types of advanced analyses can be performed in Nexus Copy Number.

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.

A New Understanding of the Genetic Basis of Pregnancy Loss: What Large-scale Cytogenomic Analysis is Revealing

It is estimated that 15–20% of clinically recognized pregnancies end in miscarriage and at least 50% of these losses result from a chromosomal abnormality.

Uniting CNV, AOH, and SV events in a Single Software System - NxClinical 3.0

NxClinical 3.0, a truly integrated system for analysis, visualization, and interpretation of data generated by both microarray as well as NGS platforms.

A new method to estimate copy number from NGS for both shallow/targeted sequencing and normal coverage WGS/WES data 

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.

Gene Prioritization in Regions of Homozygosity

This webinar is geared towards those performing genomic variation analysis and interpretation in a cytogenomics lab.

Integrated analysis of copy number, sequence variant and gene expression data in cancer cohort

This webinar is geared towards those interested in performing integrated analysis and visualization of genomic changes (copy number, sequence variants, and gene expression).

Get copy number results from WES, WGS, and targeted panel NGS with Nexus Copy Number

Watch this webinar to see just how easy and straightforward it is to import BAM files in Nexus Copy Number to detect copy number events.

An Automated Approach for Enforcement of ACMG Standards and Guidelines for CNV Analysis

NxClinical uses VIA, applying a decision tree machine learning approach for automatic pre-classification of events to be interpreted by lab personnel.