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NGS
Target enrichment panels for DNA Sequencing Sensitivity
Guaranteed promising sequencing results
Our NGS target enrichment panels demonstrate coverage and uniformity regardless of sample type:
- Robust results independent of sample quantity and quality.
- Excellent performance for GC-rich samples.
- Lot-to-lot reproducibility.
- Flexible integration on different sequencing systems.
Contact us for any questions you might have about it. We support you through the whole optimising process!
We match your application and needs
We offer ready-to-use and customised panels for diverse applications:
- Save time with an efficient detection of disease-causing genetic variants in a single NGS run.
- Accurate detection of methylation sites.
- Comprehensive analysis of tumor mutations and variants.
- Rapid and accurate viral/pathogen detection.
- Whole Exome Sequencing (WES) with >98% coverage.
Reduces errors, hands-on time, and overall processing time with its unique workflow. What is the goal of your Sequencing project? Explain it to us to support you and find out the best approach to your needs. |
Preserve and Stabilise your DNA/RNA
Get to know the gold standard buffer for DNA and RNA stabilistion:
Do you want to test it for free? Provide us your feedback!
Total RNA purified from whole blood stabilized for 24 hrs at room temperature with DNA/RNA. |
