Analyzing Cell-Free DNA from Cancer Patients to Identify 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.
Agenda:
- Align and filter whole exome sequencing data
- Detect variants from tumor and cell-free DNA
- Perform annotation and filtering to prioritize variants
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