Employing NGS Tumor Profiling To Discover Targetable Cancer Biomarkers
Research in the discovery and identification of novel, targetable biomarkers is fuelled by comprehensive tumor profiling using next-generation sequencing (NGS). However, converting tissue samples into NGS libraries is often challenging due to the low quantity and quality of DNA in such samples.
Download this app note to discover how to:
- Yield high coverage and library complexity
- Achieve highly sensitive detection of low-frequency variants
- Improve data quality
