Whatever your area of medical research, you can use the GeneReader NGS System to gain actionable insights with the GeneRead QIAact Custom Panels. Consult with us about your specific requirements and let us help you to develop a panel that will target the genes or regions of most value to your research*.

The GeneRead QIAact Custom Panels can be designed to detect all genetic variants, including somatic mutations, single nucleotide variants (SNVs), copy number variation (CNV) as well as small insertions, deletions (inDels) and fusions. Incorporating our novel unique molecular index (UMI) technology guarantees reduced variant calling errors and provides highly sensitive variant detection. As an integral part of our Sample to Insight NGS solution, the GeneRead QIAact Custom Panels are supported by QCI Analyze and Interpret, allowing seamless sequence data analysis and interpretation at the push of a button.

Each GeneRead QIAact Custom Panel contains all of the reagents required for both the target enrichment and library preparation steps of the GeneReader NGS System workflow, to help streamline your laboratory operation.