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 adoption.
From robust sample isolation and preparation tools to novel sequencing technology and advanced bioinformatics, 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 diagnostic tools 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 personalized medicine.
Wherever you are in your NGS journey—from early-stage workflow development to scaling up a high-throughput commercial sequencing operation—we’re here to work with you at every step... by phone, email, or right in your lab.
