Discover millions of predesigned assays for gene expression, mutation detection, microbial ID, and more — all optimized for real-time and digital PCR platforms.
Explore intuitive guides and resources designed to help you get the most out of GeneGlobe. Whether you're designing assays, browsing curated panels, or diving into analysis tools—find practical help to accelerate your research journey.
Developed in partnership with leading human identity labs around the world, QIAseq Investigator panels are designed to pick up where conventional STR/capillary testing cannot resolve a case. There are separate, dedicated panels for common human identify questions like biogeographical ancestry prediction, missing persons identification, or paternity testing. Focus your sequencing and data analysis efforts only on the markers of interest in your own case and increase your chances of success with QIAseq.
Highly discriminating identity SNP panel enabling kinship confirmation for challenging missing persons samples using immediate and extended family references.
The QIAseq HRR Panel has been developed as a complete Sample to Insight solution to expand HRR biomarkers beyond BRCA1 and BRCA2. The panel's digital DNA sequencing is a unique approach to detect low-frequency variants with high confidence by overcoming the issues of PCR duplicates, false positives and library bias. The panel is a one-box, NGS platform-agnostic solution that contains all the necessary components to construct libraries from enriched genomic targets. Primer design is based on single primer extension, in which each genomic target is enriched by one target-specific primer and a universal primer, a strategy that removes conventional two target-specific primer design restriction and reduces the amount of required primers. All primers required for a panel are pooled into an individual primer pool to reduce panel handling and number of pools required for enrichment and library construction. . The unique buffer and enzyme system used in the QIAseq HRR panel has been optimized to achieve high coverage of GC-rich genomic regions. Platform-specific indexes, which are contained in a separate box, allow the multiplexing of up to 384 samples per sequencing run.