Every case, fingerprinted, injury, venue, treatment, gaps, and outcome. BETA
Case Genome builds a structured fingerprint for every file in your account: injury type, venue, treatment pattern, documentation gaps, priors, and, where available, outcome. That fingerprint powers cohort matching across benchmarks, triage, and pattern features — a structuring and matching layer, not a valuation, and built only from your own tenant's cases.
A fingerprint drawn from what's already in the file.
Injury type, venue, treatment pattern, documentation gaps, and prior conditions are pulled from the record you've already processed — nothing new to enter, nothing invented. Case #IME-4812's fingerprint reflects the same 7 visits and p.140 quarantine already visible elsewhere on the file.
Matching cohorts, without matching identities.
Cases are matched to comparable cohorts by fingerprint attributes — injury, venue, treatment pattern — entirely within your own tenant. No identity, and no case content, is compared against another organization's data unless you've separately opted into a program that does that.
Powers benchmarks and triage, not a verdict.
The fingerprint is what makes Case Outcome Benchmarks and Automated Claims Triage comparisons possible — it structures and matches cases, then hands the comparison to those features. Case Genome itself never outputs a value, a rating, or a decision.
A fingerprint, not a verdict. And it never leaves your tenant.
Case Genome is a structuring and matching layer, not a valuation or decision output on its own. It compiles what's already in the file into a comparable fingerprint and hands cohort matching to the features built for that job — it never issues a number, a rating, or a call by itself.
And it's tenant-isolated: fingerprints are built and matched inside your own account. Comparing across organizations is a separate, opt-in program — Private Benchmark Network — never something Case Genome does by default.
From case file to comparable fingerprint.
Three steps, running quietly underneath benchmarks and triage.
Injury, venue, treatment pattern, gaps, and priors are pulled from the record already on file.
A structured, comparable profile for the case, kept inside your own tenant.
Benchmarks, triage, and pattern features draw comparable cohorts from the fingerprint.
Who relies on a comparable fingerprint.
Anyone who already leans on benchmarks or triage is already using this fingerprint, whether they see it directly or not.
A consistent fingerprint underneath every triage and benchmark run.
For carriersComparable cohorts drawn from within the book you manage.
For TPAsComparable prior cases surfaced from your own case history.
For law firmsA structured basis for comparing similar files at volume.
For IME orgsCase Genome, answered.
Case Genome builds a structured fingerprint for every file in your account — injury type, venue, treatment pattern, documentation gaps, priors, and, where available, outcome. That fingerprint is what powers cohort matching across benchmarks, triage, and other pattern features.
Not by default. Case Genome is tenant-isolated: fingerprints are built and matched entirely within your own account. If you want to compare against cases from other organizations too, that's Private Benchmark Network, a separate opt-in program — Case Genome never does that on its own.
No. Case Genome is a structuring and matching layer, not a valuation or decision output on its own. It feeds cohort comparisons into features like Case Outcome Benchmarks, but the fingerprint itself never issues a number, a verdict, or a recommendation.
Yes, in beta. Case Genome is live and testable now on your own case files; we're refining it hands-on with early customers, and if your use case is a good fit we'll work with you directly.
Medical Record Knowledge Graph builds the structured, cited evidence graph for a single case. Case Genome reads across that graph and other case attributes to compile a comparable fingerprint, then uses that fingerprint for cohort matching across your account's cases.
Related capabilities.
The cited evidence graph this fingerprint is drawn from.
Comparable value ranges built on Case Genome's cohort matching.
The opt-in program for comparing across organizations.
The sibling pattern layer sharpened by your own case history.
Give every case a fingerprint, kept inside your tenant.
Join the beta and see the fingerprint built from one of your own files. Handled under our BAA; never used to train a shared model.