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iFlow™ Platform

Expert-built. User‑driven.AI-powered.

iFlow is a web-based, easy-to-use platform for genomic analysis that connects seamlessly with external systems. It runs Intelliseq’s GeneSpect end-to-end workflows in a single secure environment, turning you raw genetic data into clinical-grade, reportable results ready to be signed.

See how it works
The iFlow™ Platform dashboard, showing sample, analysis and order counts alongside recent cases and analyses

how it works

Data comes in. Insights go out.Everything stays connected.

  • Data in

    Upload directly or pull from LIMS, LIS & EHR

  • Select workflow

    Choose the indication and configuration

  • Run analysis

    Automated end-to-end with QC built in

  • Review results

    Explore & visualise in VariantMINER

Results flow back to your system

Structured reports and clinical standards (HL7 & FHIR)

01 - Secure analysis environment

Genetic data.Analysed automatically.Protected at every step.

One secure platform giving access to the full spectrum of genomic workflows. Run multiple analyses on the same dataset - inside a single, fully auditable environment crafted with the sensitivity of genomic data in mind.

  • Upload once, analyse many ways. One dataset feeds multiple workflows across every indication, keeping everything unified within a single platform, free from fragmentation across multiple systems.

02 - Interoperability

Fits existing infrastructure.Connects the systemsalready in use.

Genomic data doesn't exist in isolation - and a platform shouldn't either. iFlow connects cleanly through direct integrations and open APIs, extending existing ecosystems without friction.

  • Seamless connections to LIMS, LIS and EHR platforms - data moves cleanly across the systems already in place.

VariantMINERThe workspace for expert variant review

Built for the reviewer who has to get it right the first time, not just get it done. Explore, annotate, reclassify, and sign off without switching tabs, without losing your train of thought.

The VariantMINER workspace, showing a variant's classification, evidence from external databases and gene description side by side

  • Explore detected variants

    Navigate every variant in a case through an interactive, filterable interface built for expert review.

  • Comprehensive variant annotation

    Each variant drawn together with evidence from leading databases (ClinVar, CKB Genomenon, gnomAD, FDA, OMIM) and gene-level context.

  • Expert review and curation

    Automated AMP/ASCO/CAP and ACMG classification that experts can review, override and adjust with full evidence.

  • Collaborative environment

    Multiple team members work on the same case simultaneously, aligning on findings in real time.

  • Structured reporting

    Turn reviewed variants into standards-aligned reports, generated directly from the workspace.

  • Electronic sign-off

    Securely sign reports within the platform - every signature logged, traceable and reproducible.

See iFlow™ running on real data from your laboratory

Tailored to your indication, data and the questions your team is actually trying to answer.