Are you missing the most critical information of your genome? For decades, "complete" genomes were not truly complete. Traditional reference assemblies (like GRCh38) contained hundreds of gaps, particularly in highly repetitive regions like centromeres, telomeres, and segmental duplications. These "dark regions" often hide key structural variants and regulatory elements essential for understanding evolution, disease, and complex traits.

CD Genomics brings you into the T2T era. Leveraging the synergy of PacBio HiFi high-accuracy long reads and Oxford Nanopore (ONT) ultra-long reads, we deliver Telomere-to-Telomere (T2T) Genome Sequencing services. We move beyond fragmented scaffolds to deliver chromosome-level, gapless assemblies for vertebrates, plants, and bacteria. Whether you are studying complex plant polyploidy or assembling a perfect bacterial circle, our platform reveals the full genetic picture with unprecedented continuity and accuracy.

Core Advantages:

• Close the Gaps: Resolve complex repetitive regions (centromeres, STRs) that short-read sequencing cannot touch.
• T2T-CHM13 Standards: Methodologies aligned with the breakthrough human T2T consortium standards.
• Multi-Platform Synergy: Optimized combinations of PacBio HiFi, ONT Ultra-long, and Hi-C for perfect scaffolding.