OmniFusion Engine
Integrate up to six omic layers into a single probabilistic model. Cross-evidence boosts confidence and surfaces signals no single assay can see alone.
Live
Trusted across 14 Nordic genomics centers
Illuminate the hidden biology of every diagnosis.
BeamMedic fuses genomics, transcriptomics and proteomics into a single living model — turning terabytes of raw sequence into clinical-grade answers in minutes, not weeks.
BRCA2 · c.5946delTPathogenic
TP53 · R175H
EGFR · L858RVUS · review
MLH1 · promoter
KRAS · G12CActionable
PALB2 · spliceBenign
Interpreted 1,284,907 variants · ACMG + ClinGen · 3.8 s
Whole GenomeWhole ExomeRNA-seq
Single-cellSpatialMethylation
ProteomicsLiquid BiopsyPharmacogenomics
Long-readMetagenomicsCNV / SV
Trusted by research & clinical genomics teams
Aurora BioBank
Helix Nordic
Meridian Oncology
Polaris Genomics
CellAtlas Institute
NordSeq
The platform
One model for the whole of biology.
Biology doesn't happen in silos — so why analyze it in them? BeamMedic's OmniFusion engine reads DNA, RNA, protein and epigenetic signals together, resolving the contradictions that single-omic tools miss.
The result is one coherent picture per patient: which variants matter, which pathways are disrupted, and which therapies the evidence supports — each answer traceable back to the raw read that produced it.
Genome
Transcriptome
Proteome
Epigenome
Key capabilities
Everything you need between sequence and decision.
Eight tightly-integrated modules, one audit trail. No glue scripts, no handoffs, no black boxes.
Variant Illumination
AI-assisted ACMG/AMP classification with transparent ClinGen-aligned evidence for every call.
BeamScan Pipelines
Push-button, version-pinned secondary & tertiary analysis. Reproducible to the checksum.
Spectra Atlas
Explore single-cell and spatial data in a buttery WebGL viewer — millions of cells, zero lag.
Biomarker Discovery
Find and validate multi-omic signatures across cohorts with built-in statistics and survival models.
Privacy Vault
Patient data never leaves your jurisdiction. Federated compute, end-to-end encryption, full audit log.
Clinical Reports
Auto-drafted, reviewer-ready reports with citations — exported as PDF, FHIR or HL7.
Live Collaboration
Tumor boards in real time. Comment, co-sign and share across institutions — securely.
The beam, in four steps
From FASTQ to signed report, on one rail.
STEP 01
Ingest
Drag in FASTQ, BAM, VCF or instrument output. Automatic QC, sample-sheet and contamination checks.
STEP 02
Beam
BeamScan aligns, calls and harmonizes every layer in parallel on elastic, GDPR-resident compute.
STEP 03
Interpret
OmniFusion ranks variants, maps pathways and matches evidence — every claim cited and traceable.
STEP 04
Report
Review, co-sign and export a clinical-grade report — or push structured results to your LIMS via API.
4 hMedian turnaroundFrom upload to signed report, whole genome.
99.4%ConcordanceAgainst orthogonal validation across 40k variants.
38%Higher yieldAdditional diagnoses in previously unsolved cases.
6×Faster cohortsTertiary analysis versus stitched open-source stacks.
Proof, not promises
Teams using BeamMedic in the wild.
Oncology · Tumor Board
Read the case study
Rare Disease · Trio WGS
Read the case study
Meridian Oncology cut molecular tumor-board prep from 9 days to 11 hours.
11 hPrep time
2.4×More cases / week
Helix Nordic lifted diagnostic yield 38% on previously unsolved trios.
38%Yield uplift
640+Families solved
"We replaced a stack of seven tools with BeamMedic. The first week, it flagged a fusion our old pipeline had silently dropped for two years. That's not a feature — that's a patient."
— Dr. Aino Kallio, Director of Molecular Diagnostics, Helix Nordic
Point the beam at your hardest case.
Generate a live demo report in 30 seconds, or book a walkthrough with a genomics specialist. No data required to start.