One Platform. Endless Possibilities in Genomics, Proteomics, and Beyond.
Your Gateway to Multi-Dimensional Omics
The DNBSEQ-T7’s unmatched scalability and cost-efficiency make it the perfect platform for national and global initiatives. Explore the genetic, proteomic, single-cell, and spatial transcriptomic layers of disease and health across populations - unlocking new possibilities with one powerful system.
What’s Slowing Down Your Breakthroughs?
Many researchers face recurring obstacles like high costs, manual inefficiencies, and fragmented workflows. If this sounds familiar, you're not alone.
Limited throughput leads to prolonged project timelines, delaying research outcomes.
Manual sample preparation consumes time and increases the risk of errors.
Disjointed data analysis tools complicate workflows and increase the likelihood of mistakes.
Inconsistent sequencing quality and data reliability issues impact downstream analyses.
Integrating data from multiple omics platforms is complex, resulting in fragmented insights.
High costs arise from running separate systems for spatial omics, WGS, and proteomics studies.
Take your research to new heights with seamless integration, cost-efficiency, and automation.
Fast, Flexible & Ultra High-Throughput
DNBSEQ-T7 Performance Parameter's
Whole Genome Sequencing (WGS)
Sequence up to 60 human genomes in 24 hours.
Data output
60
Flow cells
4
Data output/sample
1-7 Tb
Proteomics
Processes 344 samples per run and identifies up to 5,400 proteins simultaneously.
Data output
344
Number of proteins
5400
Spatial Transcriptomics
Processes FFPE and fresh frozen samples at Ultra-High Resolution.
Resolution
0.5 µm
Samples type
FFPE
Fresh frozen
Capture method
Random probes
Poly-A
Recommended reads
3 billion
1.5- 2 billion
Data output
4*
8*
*This is recommended samples/run. Based on sample type and quality, deeper sequencing (less sample/run) might be needed
