🎉New Product Launch | CycloneSEQ (15X) + DNBSEQ (30X) hWGS — Comprehensive Variant Detection at Scale

🎁KOL Projects | Limited-Time Promotion: Buy One, Get One Free🔥

To support large-scale population genomics studies and make precision medicine more accessible, BGI Genomics launches an ultimate solution combining long-read CycloneSEQ with short-read DNBSEQ. This cost-effective pairing enables comprehensive detection of SNP, InDel, SV, and CNV, performing comparably to PB (30X) and ONT (30X)—ideal for cohort-level studies. 🧬

📧Don’t miss this limited-time offer. Contact us to discuss study design or request a quote: info@bgi.com.