Magnis NGS Prep System offers walkaway, automated workflows for NGS library preparation with target enrichment. Requiring only 10 minutes hands-on time, the benchtop system is simple to set up. The system includes an integrated QC step to help ensure reproducibility and consistency, and generates sequencing-ready libraries for many applications, from exome to tumor genomic profiling.
For comprehensive and tumor-specific genomic profiling of cancer samples, the system is compatible with library preparation for SureSelect Cancer assays, a portfolio of assays that enable the detection of key classes of somatic variants. Starting with input as low as 10 ng DNA or RNA, targeted NGS library preparation is made easy using the Magnis NGS Prep System.
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