Copy Number Detection in Inherited Disorders and Somatic Cancer
Abstract
Copy number variants constitute a significant fraction of genomic alterations responsible for cancer and various inherited disorders. In a clinical setting, performing focused NGS testing based on a panel of relevant genes is both economical and provides faster results. Thus the ability to detect CNVs from gene panel based NGS tests increases the diagnostic yield significantly. In this webinar, we will present few clinical case studies to demonstrate the new CNV analysis workflow in Strand NGS that enables researchers to detect and visualize copy number changes ranging from single exon to chromosome level events.
Webinar Details
| Sessions | San Francisco Time (PDT) |
Tokyo Time (GMT+09:00) |
Berlin Time (GMT+01:00) |
Mumbai Time (GMT+05:30) |
| Session 1 | 25 Jun 01:30 AM |
25 Jun 05:30 PM |
25 Jun 10:30 AM |
25 Jun 02:00 PM |
| Session 2 | 25 Jun 09:00 AM |
26 Jun 01:00 AM |
25 Jun 06:00 PM |
25 Jun 09:30 PM |
