Why run FAST-RNA?
Speed & Simplicity, Without Compromise
FAST-RNA eliminates traditional NGS bottlenecks. Avoid the slowdown — no consultation rounds, no QC confirmation loops, and no custom prep delays.
7-Day Turnaround
Standardized workflow. Sequencing begins 1 day after sample receipt.
Competitive Pricing
Fixed standard specs mean lower per-sample costs, no SOW overhead.
Self-Service Ordering
No consultation required — order through our online portal (coming soon).
Raw FASTQ Delivery
Non-filtered, non-trimmed FASTQ via sFTP, ready for your pipeline.
Streamlined, Standard Process
Minimize complex back-and-forth QC communication, keeping your project on track and delivering results faster.
Free Rerun
If sequencing output falls significantly short of the target throughput, one complimentary re-run will be performed using your existing library upon client request.
SENSITIVE DETECTION, DEEPER INSIGHTS
The Paired-End Reads Advantage
Psomagen’s FAST-RNA uses paired-end (PE) sequencing, enabling:
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Full-length transcript coverage
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Richer data quality
- Gene expression & comprehensive transcript analysis
- Splicing and isoform detection
In contrast, many low-cost RNA-seq services rely on single-end sequencing, typically reading only the 3′ end of transcripts. For researchers seeking more comprehensive RNA sequencing data at an affordable cost, FAST-RNA is the ideal solution.
More RNA Sequencing Solutions
If your project requires sample QC, customized project design, or data analysis, you can explore our standard RNA sequencing services.
