Next-generation sequencing (NGS) based applications have proven to be disruptive within the clinic as well as in research. In contrast to conventional diagnostic tests, a single NGS test can identify thousands of genetic variants at once. The frequent, and still increasing, usage of NGS- based applications, resulted in the generation of mass data volumes.
Understanding how the genome is transcribed in different cell types and what changes occur when cells undergo a biological or chemical treatment leads to better insights into biology, the underpinnings of a particular disease, and possibly the success of a specific drug treatment.
Partnering with Bluebee, brings Lexogen closer to its “seamless end-to-end” approach to extract meaning from all RNA data in a smooth regimen often comprised of discrete steps involving resources that previously have not been accessible to all researchers.
Bluebee’s unique cloud-based accelerated genomics analysis platform combines best-in-class tools with a high-performance computational engine to enable efficient processing and fast, affordable diagnostics for hospitals, research centers and other clients.
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