Deep-sequencing technologies enable critical insights into all aspects of cancer genomics. In this webinar, Dr. Julie Deschenes of QIAGEN Bioinformatics, will demonstrate two comprehensive informatics solutions - CLC Cancer Research Workbench and Ingenuity Variant Analysis. These fully integrated NGS analysis platforms provide a user-friendly, and streamlined customizable solution, enabling you to easily narrow your focus to causal variants and detect and annotate low-frequency somatic variants. Experience the intuitive user interface of CLC Cancer Research Workbench, and learn how the rich biological content from Variant Analysis helps you rapidly identify critical variants in samples in this seminar.
