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:
❌ Misassignment of reads due to index hopping & cross-contamination
❌ Sequencing waste of unusable data
❌ Incorrect data interpretation and false positive data
❌ Low sensitivity, high limits of detection, unrobust sequencing assays
❌ 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 compromise:
✔️ 12-base unique dual indexes (UDI) – long and safe
✔️ ≥4 base edit distance – minimizes misassignment
✔️ Ultra-low cross-contamination – Average risk between two UDI pairs are < 0.4 reads when sequencing 10M reads
✔️ NGS performance-verified in-house
✔️ ISO 13485 medical device certification for in vitro diagnostic use
✔️ Compatible with Illumina TruSeq & NEB adapters
✔️ Scalable: Combine 4 x 96 sets to reach 384 indices
✔️ Transparent pricing: Only €299 per 96-primer set