Delivering integrated, rapid, high-fidelity long read sequencing for genotyping applications
The current state of the art for genotyping relies upon a complex set of complementary, orthogonal tools - as a result genotyping is costly, time consuming and complicated. Our approach, based on Oxford Nanopore sequencing, accelerates timelines, cuts costs, and maximises productivity.
Laverock’s Rapid Genotyping Platform (RGP) unlocks high fidelity long read sequencing on the Oxford Nanopore system, accelerating discovery and product development workflows, and replacing complex Sanger / Illumina / Long Read combination approaches.
Not only does the RGP address limitations with current approaches with a unified solution, it also integrates with your laboratory systems and workflows, providing detailed reports directly into your LIMS platform or inbox.
Our rapid genotyping platform delivers high-fidelity long-read sequencing with faster turnaround and lower error rates than conventional ONT workflows, transforming the pace and precision of discovery.
Genotyping is critical in genome editing to:
But legacy methods are slow and fragmented.
A single, in-house platform using ONT long-read sequencing, optimised for accuracy and speed delivers:
One platform for pooled & clonal analysis.
