Domlan Diagnostics - Molecular Pathology & Genomics Unit
Specialist reference laboratory providing molecular oncology and cancer biomarker diagnostics
The Everyday Challenge
Complex molecular assay results and biomarker reports required labor-intensive manual translation into oncologist-friendly clinical summaries.
How They Use Ireti
Processes raw molecular assay outputs and genomic mutation panels (EGFR, KRAS, BRAF, HER2), structuring variant data into traceable clinical summaries directly accessible to referring oncology networks.
Their Output & Impact
Zero transcription errors in molecular biomarker handoffs, instant automated matching against NCCN/ESMO evidence guidelines, and direct digital reporting to 120+ referring cancer specialists.
3x faster handoff of complex biomarker reports; 120+ clinical oncology teams receiving structured genomic summaries.
“Bridging the gap between our molecular genetics analyzers and the oncologist's desk has drastically accelerated precision therapy matching.”
How the work comes together
- 01
Keep the source close
Review an extracted finding alongside the original report, with a page reference.
- 02
Spot what is missing
Flag incomplete dates, missing fields, and conflicting findings before the case reaches review.
- 03
Approve the case record
A clinician checks the structured findings before the record is used.
Capabilities used: Pathology & Molecular Evidence, Research, Care Coordination
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