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Pioneering
the integration of
DNA & RNA sequencing data with AI for
rare disease diagnostics

We offer the first RNA-based diagnostic support tool

for rare disease patients that remained

undiagnosed after DNA-based tests

Phitech-MainPage-Image.png
Phitech-MainPage-Image.png

The First RNA-Seq-based, AI-powered 

Diagnostic Decision Support Platform

for Rare Diseases

Get in touch

How can we help you?

Leveraging the additional diagnostic power of RNA-Seq data, we extract and deliver critical information on these,
to support your diagnostic decisions

Pathogenic
Variants
Aberrantly Expressed
Genes & Transcripts
Monoallelically
Expressed Genes
Aberrantly
Spliced Genes
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