BioDiscovery Webinars

Topic: Cancer Research

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.

Application of ASCAT Processing to Tumor Samples Using Nexus Copy Number

Analyzing copy number variation in cancer tissues can be a difficult task, but Nexus Copy Number can help!

Improving Your Research Results – Getting the Most Out of Nexus DB

Get an overview of Nexus DB for querying specific changes to identify recurrent events in other data sets, identifying secondary data sets for results validation, and integration of available data on Nexus DB with your current analysis.

TCGA Premier – Curated CNVs for improved, efficient, and more accurate analysis

Learn how to access and make use of TCGA data, and easily query and analyze data sets, and much more.