BioDiscovery Webinars

Product: Nxclinical

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.

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.

Gene Prioritization in Regions of Homozygosity

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

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.

Evolution Of Software Tools For CNV Interpretation

NxClinical 2.1 is a revolutionary tool single integrated platform-independent solution that manages the entire data processing experience. Learn more.