Whole Genome Sequencing- as low as $350
Want to get first access?
Access Illumina's most advanced sequencing technology today
Broad Institute will be the first to offer services using the NovaSeq X Plus series.
The NovaSeq X Plus system offers Illumina's most advanced, powerful sequencing yet, providing scalability and ultra-high throughput using upgraded flow cell density and optics resolution. Discover improved genome coverage, greater %Q30 scores, reduced base-specific bias, and improved sensitivity for indels and SNPs. Reach out to us to learn more about the new and improved technology.
Coming April 2023
Whole Genome Sequencing for as low as $350
WGS has never been faster or more affordable. The NovaSeq X series platforms have an output of up to 52 billion reads per run. Improved on-board sequencing chemistry and analytical technology yield:
+ higher throughput
+ greater accuracy
+ faster run time
As part of our commitment to providing unsurpassed excellence in sequencing, the Broad Institute now offers services utilizing the improved capabilities of the Illumina® NovaSeq X platform.
- Improved genome coverage
- Greater %Q30 scores
- Reduced base specific bias
- Improved sensitivity for indels and SNPs
Walk-Up Sequencing
Looking for a quick and easy sequence data generation and delivery service for pre-constructed DNA libraries? We now offer the NovaSeq X Plus platform for our Walk-Up sequencing customers.