Analyzing Cell-Free DNA Seq Data from Cancer Patients to find Actionable Variants

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Webinar:
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

Live Sessions Offered:

• September 27, 2017 at 10am SGT (Singapore)
• September 28, 2017 at 2pm GMT (London)
• September 28, 2017 at 2pm EDT (Boston)

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