The problem
NGS Multiplexing Without a Safety Net
Multiplexing is a smart way to reduce sequencing costs — but it comes with risks.
If you're experiencing any of the following issues, you're not alone:
❌ Index hopping
❌ Cross-contamination
❌ Misassignment of reads
❌ Unpredictable results and re-runs
❌ Long delivery times or inflexible set combinations
Scientists today are under pressure to deliver clean, reproducible data — and compromised index primers are a common root cause of unreliable sequencing results.
OUR SOLUTION
UDI Primers That You Can Trust
Eurofins Genomics’ NGS UDI Primer Sets offer a reliable way to safely multiplex without compromising on precision:
✔️ 12-base unique dual indexes (UDI) – long and safe
✔️ ≥4 base edit distance – minimizes misassignment
✔️ Ultra-low cross-contamination – just 0.0014% in real-world sequencing
✔️ NGS performance-verified in-house
✔️ Certified under ISO 13485
✔️ Compatible with Illumina TruSeq & NEB adapters
✔️ Scalable: Combine 4 x 96 sets to reach 384 indices
✔️ Transparent pricing: Only €299 per 96-primer set