The GeneReader platform redefines the NGS workflow by providing unmatched batching flexibility with multiple flow cells (1-3). Its inventive turntable design makes it possible to sequence multiple samples (up to 42 samples at a time) independently and in a parallel or staggered manner. Random access, scalability and cost-efficiency mean that you can process samples when needed instead of when allowed by the sequencer. The GeneReader sequencing instrument is fully embedded into the Sample-to-Insight GeneReader NGS System.

The GeneReader platform is now available for use with an expanded targeted gene panel menu, including the GeneRead QIAact Actionable insights Tumor, BRCA 1/2 and Lung DNA panels, covering copy number variants (CNVs), SNVs and Indel variants, to provide deeper cancer research insights than ever before.