Advance disease research with the QIAseq Human Exome Kit, which leverages hybrid capture technology for highly sensitive variant calling of targets of >500 genes. Seamless integration with QIAGEN CLC Genomics Workbench enables rapid variant calling and QIAGEN Clinical Insight Interpret (QCI-I) ensures accurate variant interpretation and disease-specific insights – without the burden of manual curation. This time-saving solution results in a 50% reduction in sequencing costs per sample and decreases overall turnaround time from sample to data by 40%. Access the previously inaccessible with ease using our exome sequencing solution.
QIAseq FX library prep (enzymatic fragmentation)
Exome enrichment (single-plex or 8-plex hybridization)
Go from raw reads to variants in 60 min, speed up with multi-node analysis
Insight Interpret (QCI-I)
Confidently report on pathogenic variants in minutes
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