You don’t need to be an NGS expert to begin using genomic tools in drug discovery. Illumina offers guided onboarding, intuitive workflows, and extensive training resources to help teams ramp up quickly. Many of the most common pharma R&D applications such as targeted DNA/RNA sequencing, mRNA analysis, and single‑cell methods are already well‑established and available as intuitive, end‑to‑end workflows.
If you're new to sequencing, our NGS for beginners resources provide step‑by‑step guidance on choosing the right platform, preparing samples, and interpreting results. Illumina specialists and global support teams are also available to help you design your workflow, scale at your own pace, and ensure you get quality data from day one.