BioDiscovery Webinars

Topic: Cytogenetics

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.

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.

Whole Genome MAQ in Nexus Copy Number software – A fast, simple, and integrated tool for CNV validation

Bert Eussen gives some helpful hints for those studying copy number variation from arrays or NGS and need an alternate method for validation of CNVs.

Genomic studies of neurodevelopmental disorders: the move from arrays to sequencing

In this webinar, we will examine a few different cases of early-onset epilepsy and hyperphosphatasia with intellectual disability, better known as Mabry syndrome, an autosomal recessive form of ID.

Constitutional and Cancer Sample Review for Cytogeneticists: Copy Number and Sequence Variant Analysis Using Nexus Copy Number

Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.Learn how CNV, LOH and sequence variant analysis tools for cytogeneticists allow for better decisions on the significance of events being detected.