BioDiscovery Webinars

Topic: Copy Number

Increasing the yield of whole exome sequencing (WES) with copy number variant (CNV) analysis

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

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!

Investigation of the TCGA LAML dataset using Nexus Copy Number

Learn how to identify relevant common events within the TCGA project and how to leverage the clinical information provided for the samples.

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.