3-day TAT
Whole genome
Complete genomes for any organism.
Whole genomes, exomes, transcriptomes and microbiomes — sequenced, analyzed and delivered on one platform with industry-leading turnaround.
Six core services, one submission flow.
Prep, drop, done. No instruments, no capital, no queue to manage.
Annotated, interactive results you can act on — not just raw FASTQs.
Collection points and labs across Asia, Europe and North America.
Complete genomes for any organism.
Deep coding-region coverage for variant discovery.
Expression, splicing and fusion detection across the transcriptome.
Species-level identification from raw environmental samples.
Resolve cellular heterogeneity one cell at a time.
Focused, cost-efficient panels for known targets.
Four steps from bench to answer.
Register and enter any number of samples in minutes.
Drop at a nearby collection point or use a prepaid label.
NovaSeq X and long-read platforms run around the clock.
Annotated results and raw data land in your dashboard.
Researchers at 2,000+ institutions run on Fast Track.
“Data back before our next lab meeting. Fast Track changed how we plan experiments.”
“Publication-grade accuracy with a turnaround we did not think was possible.”
“One submission flow for WGS, RNA-Seq and microbiome. It just works.”
Create an account and submit your first sample today.
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