Overcoming sequence artifacts to fuel clinically relevant NGS applications

This webinar introduces Watchmaker Genomics’ enzymatic DNA library prep and amplification solutions designed to address common challenges in NGS, including sequence bias, fragmentation artifacts, and polymerase error.

• Reduce common sequencing artifacts such as chimeric reads, hairpins, and polymerase-induced errors.
• Obtain consistent library prep performance across a wide range of DNA input amounts, with adjustable fragmentation settings.
• Improve data quality through low-bias enzymatic reagents and uniform amplification, supporting reliable variant detection.