5 Key Takeaways

• 1

  The Magnis NGS Prep System automates workflows for NGS library preparation with target enrichment.

• 2

  It requires only 15 minutes of hands-on time and is easy to set up on a benchtop.

• 3

  The system includes an integrated QC step to ensure reproducibility and consistency in results.

• 4

  It generates sequencing-ready libraries suitable for various applications, including tumor genomic profiling.

• 5

  The system supports library preparation for SureSelect Cancer assays, starting with as little as 10 ng of DNA or RNA.