How to Analyze Cell-Free DNA Sequencing Data from Cancer Patients to Identify Clinically Actionable Variants
In this webinar, whole exome sequencing data of tumor tissue and cell-free DNA derived from two cancer patients will be used to demonstrate how non-invasive liquid biopsies from the blood have the potential to aid in precision medicine. Using Partek® Flow® software, a powerful and easy-to-use bioinformatics tool, we will analyze raw sequence data from individuals with metastatic sarcoma and metastatic breast cancer to identify clinically actionable variants.  
You will learn how to:
Align and filter whole exome sequencing data
Detect variants from tumor and cell-free DNA
Perform annotation and filtering to prioritize variants
Session One
September 27, 2017
10:00 A.M. SGT - Singapore
Session Two
September 28, 2017
2:00 P.M. GMT - London
Session Three
September 28, 2017
2:00 P.M. EDT - Boston
Content is identical in all sessions