As sequencing platforms like the Complete Genomics DNBSEQ-T7+ and DNBSEQ-T1+ continue to scale, generating terabytes of high-quality data faster than ever, the primary bottleneck in genomics has shifted from data generation to data analysis.

Traditional CPU-based workflows can take hours per sample, limiting the pace of discovery and real-world clinical utility.
Building on our previous webinar with Google AI, which highlighted how pangenome-informed, AI-driven Google DeepVariant enables highly accurate variant detection on the DNBSEQ-T7+, this webinar will focus on breaking the compute bottleneck once and for all.