FynSig Contact us
FynSig logo: a protea inside a hexagon FynSig

Find and describe even the smallest cells

FynSig specialises in computer vision and is based in Stellenbosch, South Africa. The name “FynSig” translates from Afrikaans as fine sight. Fittingly, our first product is an image-based flow cytometry platform that excels at finding and describing even the smallest of cells.

What makes us different

The first flow cytometry analysis platform powered by instance segmentation

Extract richer data

Every cell becomes its own object, with its own shape, size and texture — not just a point in a gate.

Discover more in analysis

Measurements you could not make before, on populations you could not separate before.

Get results faster

Automated where it used to be manual, so analysis stops being the thing you wait for.

Beta — Q2 2027

Struggling with a data backlog?

So were we, until we started optimising and automating. We are looking for early adopters of our beta, coming Q2 2027.

R9M

Yearly operating cost of a flow cytometry lab

Analysis takes twice as long as acquisition

3,000

Hours spent on analysis per year

R720K

Annual bioinformaticist wages spent on analysis

The platform

Built with images in mind

Our platform is designed specifically for imaging flow cytometry. Haven't upgraded yet and still using a conventional flow cytometer? No problem — it handles old-school flows just as well.

  1. Raw FileAny imaging flow cytometry image
  2. SegmentationInstance-level AI cell detection
  3. QuantificationRich image feature extraction & classification
  4. SignificanceBuilt-in statistical tests, ready for publication

Old flows welcome

Conventional, non-imaging cytometers are supported too. You do not need new hardware to start.

Machine learning built in

Find deeper relationships in your data and classify it, without leaving the platform. No tiers, no extra subscriptions.

Fast processing

Our model handles 600 images per second and is small enough to run on your laptop.

See for yourself

The images below contain blood cells captured on an imaging flow cytometer, view them three ways. To a machine each colour is one detected cell. Our model identifies each cell as its own entity, even when part of a clump.

Raw brightfield frame with several cells, some touching The same frame segmented by FynSig, each cell a separate colour The same frame segmented by traditional thresholding: one mask covers every cell, and touching cells merge
Raw brightfield frame with several cells, some touching The same frame segmented by FynSig, each cell a separate colour The same frame segmented by traditional thresholding and watershed

Interact with data

The same 100 events are measured two ways. FynSig sees every cell as its own distinct entity. Drag the slider to switch between them, and point at any dot to see the cell behind it.

Traditional Methods
FynSig Model

Contact us

Like what you see? Get in touch.

Tell us what you are trying to measure and what is slowing you down.

info@fynsig.com
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