DeepFCS reads flow cytometry
like never before.
Every population found, gated and named — every finding traced back to its markers. No manual gating. No guesswork. In seconds.
DeepFCS reads
every marker.
Not a chosen few — where a cytometrist reads a population on a gate, DeepFCS reads every event on every marker your panel carries, each antigen weighed as evidence, not a checkbox.
| CD34 | CD38 | CD7 | HLA-DR | |
|---|---|---|---|---|
| Blast | + pos90.9%440,119/484,424 | + pos99.7%482,976/484,424 | − neg0.1%289/484,424 | + pos95.6%462,908/484,424 |
| Lymph | − neg0.0%6/61,156 | + pos52.4%32,041/61,156 | + bright70.8%43,316/61,156 | + bright26.5%16,230/61,156 |
| Mono | + bright54.0%2,258/4,184 | + pos93.5%3,910/4,184 | + bright36.8%1,538/4,184 | + bright58.1%2,430/4,184 |
| Gran | · n/a— | · n/a— | · n/a— | · n/a— |
| Total | 80.5%442,383/549,764 | 94.4%518,927/549,764 | 8.2%45,143/549,764 | 87.6%481,568/549,764 |
Thousands of events.
Nothing missed.
Every cell that crosses the laser, DeepFCS accounts for — exceptional on BD today, with more instruments on the way.
| Population | Events | % |
|---|---|---|
| Lymph | 7,685 | 76.8% |
| Gran | 1,323 | 13.2% |
| Blast | 856 | 8.6% |
| Mono | 136 | 1.4% |
| Total | 10,000 | 100% |
Signal becomes identity.
From scatter and fluorescence, DeepFCS reconstructs what each cell actually is — built to EuroFlow and WHO standards.
It gates itself.
No manual quadrants. DeepFCS resolves lymph, mono, gran and blast on the CD45 × SSC backbone — the read it does best today — finding, naming and counting every population.
Into a single
population.
DeepFCS doesn't stop at the map. It dives into one population — every lymphocyte read on its own surface markers.
And splits it again.
Within the lymphocytes, distinct sub-populations resolve — proportions, clonality, the cells that matter. Precision once thought out of reach.
Many minds,
one read.
A multi-layered Cellular Intelligence — dozens of specialised models and agents, each reading the cells from its own angle and cross-checking the others. Every finding traces back to its markers.
From upload to result.
Every step is explicit — nothing hidden, nothing assumed.
Secure upload
Your FCS file is uploaded over an encrypted channel and stored encrypted at rest.
Anonymization
Patient identifiers are stripped before analysis. DeepFCS never needs — or sees — who the patient is.
Quality control
Instrument and panel detected automatically, scaling normalized, debris and doublets filtered out.
Population discovery & auto-gating
Every population is found, gated and named on the CD45 × SSC backbone — lymph, mono, gran, blast and CD34⁺ stem / progenitor cells — with no manual quadrants.
Immunophenotyping & marker interpretation
Every marker on the panel is read per population — positivity graded by intensity, clonality (κ:λ), aberrancy and MRD signals weighed as evidence.
Disease evidence scoring
Population-aware, exclusion-sensitive scoring built to EuroFlow and WHO standards — difference-from-normal, never a black box.
Review & correct
Not convinced by a read? Adjust a gate or a quadrant cursor in the built-in editors — the populations, counts and evidence re-compute on the spot, and the call stays yours.
Summary & report
A traceable disease summary and PDF — every finding linked back to its markers. In seconds.
A disease summary,
built for the clinician.
Competing diagnoses, an honest confidence state, and the markers behind each — transparent. And meet Nova, the built-in analysis assistant: it reads the case and explains the evidence in plain language, every claim tied back to its markers. The call stays yours.
Start when you're ready.
Scale as you grow.
Subscription credits — pick the tier that fits your lab.
Normal
- Core analysis
- PDF report
- 1 user
Pro
- MRD + Disease Summary
- Nova assistant
- Priority support
Max
- API access
- Team / multi-user
- Priority compute