In exclusive clinical partnership with KPCIRC
OnKommon

Turn existing data into a decision

Decipher

Already tested elsewhere? We turn data you already have into a full Blueprint Care decision, with no new sequencing.

01Turn existing data into a decision

Already tested elsewhere?

Decipher turns data you already have into a full Blueprint Care decision, with no new sequencing. We run your existing genomic report through our engine and KPCIRC sign-out.

You get the ranked plan, the trial matches, the biosimilar and access mapping, and the six intelligence layers, built on the test you already paid for.

0new samples needed
6intelligence layers applied
1signed decision
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An old report becoming a new plan

What goes here: Photograph of a patient handing over a folder of existing lab reports across a desk, with a laptop showing the OnKommon report open beside it. The idea to convey is reuse, not repetition. Warm, ordinary, unstaged.

02

When it is right

You have a variant list

A recent comprehensive report, but no decision attached.

You want a deeper read

A second, more thorough interpretation and a signed plan.

You want to avoid re-testing

No cost or delay where re-sequencing is not needed.

03

Decipher or Decipher Plus?

DecipherDecipher Plus
What we doInterpret your existing data in fullInterpret, and fill only the missing pieces
New testingNoneA targeted top-up only, such as TMB, MSI or PGx
Best whenYour report is comprehensiveYour report is missing markers
OutputFull Blueprint Care reportFull Blueprint Care report

04

How it works

  1. Step 1Share your report

    Send us your existing genomic results.

  2. Step 2We assess completeness

    We identify whether anything essential is missing.

  3. Step 3Interpret, and top up if needed

    Decipher reads as-is. Plus adds the gaps first.

  4. Step 4KPCIRC sign-out

    You receive a full, signed decision.

05

Quality in, quality out

We will not present an incomplete picture as a complete one.

Decipher can only interpret what your existing data contains. If your report is missing markers we will recommend Decipher Plus rather than fill the gap with guesswork.

Being clear about our limits

What we do and do not do

What we DO

  • Re-annotate every alteration against current knowledge
  • Apply all six intelligence layers and match trials, biosimilars and access
  • Return a complete, tumour-board-signed decision
  • Tell you honestly when your data is not complete enough

What we DON’T do

  • Diagnose or decide treatment on its own
  • Interpret markers your original report never measured
  • Present an incomplete picture as complete
  • Guarantee drug availability, approval, cover or benefit
Plain-language glossary (4 terms)
TermWhat it means
InterpretationTurning an existing variant list into a ranked, evidenced decision.
Top-upA small, targeted test to fill one missing marker such as TMB, MSI or PGx.
MTBMolecular tumour board, the licensed panel that signs the final decision.
VUSVariant of uncertain significance, a change whose meaning is not yet clear.
Important information and regulatory status

Take the next step

Three ways forward. Pick the one that fits today.

01

Book a free consultation

A no-obligation conversation with our care team, arranged through KPCIRC.

Book a consultation
02

Begin Blueprint Care

Commission your decision report and a dedicated clinical team.

Explore Blueprint Care
03

Ask on WhatsApp, free

Signal replies to your first question within four hours, at no cost.

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