Built & deployed · seven clinical tabs live

From a blood draw to a decision, in one platform.

CellWise outsources the wet lab and does the hard part in software: turning a high-dimensional single-cell dataset into a structured, clinician-ready read, with the quality control and population context that makes it defensible.

✓ Built and deployed, not a concept ✓ Seven clinical modules live ✓ Schema-validated, free of AI hallucination
CellWise · Pipeline
Status
Deployed
Modules live
7 / 7
From one PBMC draw
400+
biomarkers
Resolution
Single-cell
Health domains
9
risk-rated domains
Sample to decision
Sequencing · single-cell CRO
QC + population normalization
Seven analysis engines
Report + surveillance
Precision input to precision output
Raw single-cell expression, delivered as a decision you can act on.
Grounded inreal population datapeer-reviewed researchlegacy single-cell technology
The Founding Practitioner Pilot: up to five of your own patients at $1,485 each for Core Plus, 29% below standard, invoiced only for the ones you send.
See the terms
How it works

How a sample becomes a decision.

CellWise stays software-only. The wet lab happens at a CRO; everything that turns raw data into a clinical read happens here.

Step 01

Sequencing

The sample is run through a single-cell licensed CRO. CellWise never touches a wet lab, so there's nothing new to build or staff.

Step 02

QC + normalization

Strict filtering removes apoptotic cells, and MAD statistics normalize the donor against a dynamic population baseline, eliminating batch effects while preserving rare signal.

Step 03

The engines

Seven modules read the cleaned data: phenotyping, the peptide atlas, the aging profile, target mapping, and more.

Step 04

Grounded report

Findings are drafted as a narrative, then reconciled against curated genomic data, population and individual, and held to a strict schema, so every statement is grounded in the data, not model guesswork. The clinician-ready report pipes into your existing portal, with surveillance between screens.

Everything in the portal

Seven modules, one clinical workspace.

Health Analysis Report

The clinical home base. Use-case assessments, immuno-metabolic phenotyping, the therapeutic target map, stress profiling, and more, all in one report.

Biomarker Analytics

The quantitative, visual view of the patient's raw biomarker data, shown as a population-vs-patient overview.

Data Explorer

A filterable, gene-level interface over the patient's complete dataset, exposing the top cell populations carrying each signal.

Clinical Scenario Simulator

Test a clinical hypothesis against the patient's own molecular data and re-run it in seconds.

Outcomes & Monitoring

Assay-independent surveillance across dosing phases, peptide-specific labs, and wearable trends, with no repeat sequence required.

Cellular Aging Profile

Immune age, senescence, and the 12 hallmarks from one PBMC sample, for cell-resolved biological aging.

Δ

Longitudinal Screening

Re-assay a patient and see the gene-expression deltas across key biomarkers, so you see what has shifted since the last screen.

Under the hood

The capability, in numbers.

What the platform reads, ranks, and connects to.

400+
Biomarker genes across immune cell populations, the resolution bulk panels average away.
519 alert rules
Post-therapy alert rules across 88 peptides, drawn from regulatory and clinical efficacy data and feeding the live surveillance feed. Compatibility ranking is separate and runs against commercially available peptides.
MAD
Median-absolute-deviation normalization against a population baseline, so results hold across runs.
Schema locked
Every finding is reconciled against curated genomic data and held to a strict JSON schema, so reports render from the data itself, free of AI hallucination.
AI
A scenario simulator anchored to the patient's own molecular data, for hypothesis testing in seconds.
7
Clinical modules, live and deployed today, from the health report to longitudinal screening.
Scope of use

Research use only, and decision support.

Two things about CellWise that are easy to skim past, so we state them plainly on the page rather than only in the footer. The literature the panel was curated from is listed on the references page.

RUO

Research use only

RUO means research use only. CellWise is a software-as-a-medical-device on a clearance pathway and has not been cleared or approved by the FDA. Until SaMD clearance it is for research use, it is not a diagnostic, and it is not intended to diagnose, treat, cure or prevent any disease.

Decision support

It informs a decision, it does not make one

CellWise is decision support for a licensed practitioner. It organizes molecular evidence and shows the reasoning behind every call, including the reasons against. Every diagnostic and treatment decision stays with the clinician and their patient.

What we do not claim

No outcome is promised

Expression is reported against a population baseline whose version is printed on every report, and that baseline grows as samples accumulate, so reported ranges may be revised. CellWise makes no claim that a report is diagnostic, that the baseline is final, or that any clinical outcome will follow.

Help us shape it.

We're onboarding a limited group of design partners to build the platform with. Free proof-of-concept, founder pricing, and a direct line to the team.