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Platform · Genomics

Genomic insight, prepared for physician review

WGS and targeted mutation analysis turned into clear health profiles, diet and lifestyle guidance and treatment-plan suggestions — each one reviewed and approved by a physician.

From sample to report

A clear path with a physician at the end of it

  1. Step 1

    Sequencing

    Whole genome sequencing or targeted panels, run in the partner lab's own workflow.

  2. Step 2

    Analysis

    Variants are identified, annotated and classified against curated references.

  3. Step 3

    Structured report

    Findings are organised into a health profile written for clinicians.

  4. Step 4

    Physician review

    A physician reviews, edits and approves before anything reaches a patient.

Report preview

Built to be read quickly and reviewed carefully

A variant summary, a region view, and guidance sections that are clearly labelled as pending physician review.

Genomic health profile

Whole genome sequencing summary

Prepared for physician review

Pending physician review

Variant summary

Structure of the variant summary in a genomics report
ClassificationWhat the reviewer seesStatus
Flagged for physician reviewEvidence summary, inheritance and referencesReview required
Uncertain significanceCurrent evidence and reclassification notesClinician judgement
Likely benignListed for completenessFor information

Region view

Likely benign Uncertain significance Flagged for physician review

Health profile

Summary of relevant findings, written for clinicians.

Diet & lifestyle

Guidance considerations for discussion with the patient.

Treatment suggestions

Options for the physician to review — not a prescription.

Interpretation and any clinical action rest with the ordering physician.

Illustrative example — not real patient data.

Visualisation

Context at every scale

From a genome-wide overview to an individual gene region, visual context helps reviewers orient themselves.

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Genome overview with a highlighted region of interest.
Likely benign Uncertain significance Flagged for physician review
Structure of the variant summary in a genomics report
ClassificationWhat the reviewer seesStatus
Flagged for physician reviewEvidence summary, inheritance and referencesReview required
Uncertain significanceCurrent evidence and reclassification notesClinician judgement
Likely benignListed for completenessFor information
Region view and variant summary structure.

Illustrative example — not real patient data.

Outputs

What reviewing physicians receive

  • Variant interpretation

    Clear classification of variants of note, with the supporting evidence summarised for the reviewer.

  • Health profiles

    A structured overview of relevant findings, organised by area so it is quick to review.

  • Diet & lifestyle guidance

    Considerations a physician can discuss with the patient, framed as guidance rather than prescriptions.

  • Treatment-plan suggestions

    Options for the physician to weigh alongside the full clinical picture. Never sent directly to patients.

FAQ

Common questions

Who sees the report first?

The reviewing physician. Reports are prepared for physician review and are not released until a clinician has approved them.

Are treatment suggestions instructions?

No. They are options for the physician to consider alongside the patient's history, preferences and other results. Clinical decisions remain with the physician.

Can reports be adapted to our lab's format?

Report structure and branding can be configured with partner labs during onboarding.

Learn more

The science of the sequence

DNA, sequencing and what genetics can — and cannot — tell you, with cited sources.

Talk to us about genomics in your lab

Book a walkthrough with our team. We'll show how doctor-in-the-loop decision support fits alongside your existing systems, and answer your clinical, technical and governance questions.