Book a free consultation
A no-obligation conversation with our care team, arranged through KPCIRC.
Book a consultationTurn existing data into a decision
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
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.
An old report becoming a new plan
02
A recent comprehensive report, but no decision attached.
A second, more thorough interpretation and a signed plan.
No cost or delay where re-sequencing is not needed.
03
| Decipher | Decipher Plus | |
|---|---|---|
| What we do | Interpret your existing data in full | Interpret, and fill only the missing pieces |
| New testing | None | A targeted top-up only, such as TMB, MSI or PGx |
| Best when | Your report is comprehensive | Your report is missing markers |
| Output | Full Blueprint Care report | Full Blueprint Care report |
04
Send us your existing genomic results.
We identify whether anything essential is missing.
Decipher reads as-is. Plus adds the gaps first.
You receive a full, signed decision.
05
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
| Term | What it means |
|---|---|
| Interpretation | Turning an existing variant list into a ranked, evidenced decision. |
| Top-up | A small, targeted test to fill one missing marker such as TMB, MSI or PGx. |
| MTB | Molecular tumour board, the licensed panel that signs the final decision. |
| VUS | Variant of uncertain significance, a change whose meaning is not yet clear. |
Decipher and Decipher Plus is a genomic (DNA-based) test for use by qualified healthcare professionals. It supports clinical judgement, it does not replace it, and it must be read alongside your full clinical history and applicable guidelines.
Regulatory status (India). Registration of our genomic tests as in-vitro diagnostic (IVD) medical devices with CDSCO is in progress, with the IVD class pending. Sequencing and variant calling are done by an accredited laboratory partner (CAP-accredited, ISO 15189) following ACMG/AMP/ASCO/CAP guidelines and a CE-IVD certified variant database. The OnKommon interpretation engine is provided for research and decision-support use. Marketing follows the Drugs and Magic Remedies (Objectionable Advertisements) Act, 1954.
Take the next step
A no-obligation conversation with our care team, arranged through KPCIRC.
Book a consultationCommission your decision report and a dedicated clinical team.
Explore Blueprint CareSignal replies to your first question within four hours, at no cost.
Start with Signal