Latest improvements to the GeneReader NGS System
We are pleased to announce the latest additions to our GeneReader Sample to Insight System, including the release of the QIAact Myeloid DNA UMI Panel:
The main highlights are:
- Detection of SNVs and InDels
- High detection sensitivity for variants in JAK2 and KIT (1% VAF), KIT D816V (0.4% VAF), enabled by digital sequencing using UMIs
- Detection and reporting of challenging mutations including FLT3 ITDs, CALR deletions and CEBPA mutations
- Automated bioinformatic analysis and reporting with QCI Analyze
For further information on the panel, please visit the
QIAact Myeloid product page