NGS
Comprehensive — but out of reach
- Biomarkers
- Thousands
- Turnaround
- ~4 weeks
- Cost
- > $3,000
Massively multiplexed qPCR
VibrantBio fuses nanofabrication with biology to put NGS-scale genotyping on a single qPCR chip — the breadth of sequencing at the cost and speed of a routine lab test.

The unmet need
Targeted therapy depends on knowing a tumor’s mutations. Yet today every lab must trade breadth for speed and cost — so broad genomic testing reaches only a fraction of the patients it could help.
Comprehensive — but out of reach
Fast & cheap — but narrow
The result
Only ~2% of patients receive large-panel genetic testing — while an estimated 800,000 per year would benefit. VibrantBio closes that gap.
The technology
Two breakthroughs make 2,000-plex qPCR possible on one chip: a microfluidic array of 50,000 isolated reactors, and color-coded VibrantBeads that tell each reactor what it is testing.
Component A
A nanofabricated array packs 50,000 sealed wells onto a 4×4 cm chip. Each well isolates one reaction, so the same reporter dye works everywhere and thousands of tests run without interference.
Component B
Microbeads doped with up to 20 spectrally resolvable Raman probes generate over a billion unique barcodes. Each bead delivers a known primer pair and an address the imager can read.
VibrantBeads® carry primer pairs and are tagged with narrow-linewidth Raman dyes — combined to yield billions of distinct optical barcodes, far beyond what fluorescence allows.
Beads fall randomly, one per microwell, across 50,000 wells. A self-priming chip draws the sample in with a single pipette — no instruments, no fluidics.
Each well is a sealed microreactor running standard qPCR in parallel — compartmentalization removes the primer cross-talk that caps conventional multiplexing at ~10 targets.
A large-field-of-view imager captures every amplification curve in one shot. Software maps each barcode to its target and returns a per-gene report.
Proof of concept
This is not a concept on a slide. We have demonstrated every core component — the barcoded beads, the microreactor array, and the single-shot imager — and run massively multiplexed screens against known truth.
Backed by a decade of multiplexing research · 10 patents filed, 2 published
The opportunity
Genomic cancer testing is growing past 22% a year as targeted therapy becomes standard of care. The bottleneck is not demand — it is the cost and speed of today’s tools.
New cancer diagnoses
20M
per year, globally — each a candidate for genomic profiling.
Current penetration
~2%
take large-panel testing today — the runway is the other 98%.
Growth
22%
CAGR across genomic cancer panels and profiling.
Competitive landscape
Others optimize for breadth or for cost. VibrantBio is the first to deliver high multiplexing, low cost, and fast turnaround at once.
| Platform | Method | Cost efficiency | Turnaround | Multiplexing |
|---|---|---|---|---|
| VibrantBioUs | Multiplexed qPCR | |||
| Illumina (NGS) | Sequencing | |||
| Fluidigm | Microfluidic qPCR | |||
| AplexBio | Nucleic acid | |||
| ChromaCode | Nucleic acid | |||
| Thermo, Bio-Rad | Nucleic acid | |||
| Luminex | Affinity / protein |
Built for
Run NGS-scale tumor panels in-house in 30 minutes, without sending samples out or waiting weeks for results.
A pipette-and-go workflow brings broad genetic pre-screening to clinics that could never run NGS.
High-throughput, low-cost panels for large diagnostics operations — the economics to test at population scale.
Roadmap
Get in touch
Investors, partners, and labs — tell us why you’re reaching out and we’ll get back to you quickly.
info@vibrantbioscience.com