At Roche we are working to make next-generation sequencing simple and accessible enough for routine use. By accelerating clinical research, streamlining workflows and expanding assay menus, we are broadening access to genomic data and lowering barriers to routine use.
From strong sample isolation and preparation tools to novel sequencing technology and advanced informatics, we are developing differentiated, highly integrated end-to-end solutions for next-generation sequencing, resulting in a sample in, result out workflow.
We are dedicated to creating diagnostics and developing techniques that are tailored to individual genetic and disease profiles, meeting the demands of research and clinical practice to deliver on the promise of personalised medicine.
