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GeneLens

The genetic report, read against the medicines the patient is actually on — and a hereditary cancer family’s cascade testing.

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What it is

A genetic report arrives as a PDF and is filed. This puts it beside the prescription. The report is recorded as the laboratory issued it — its reference, its panel, and each finding in the laboratory’s own words — and the gene-drug flags are computed where three things meet: a finding that states a phenotype, a rule in the pharmacogenomic table this hospital has loaded, and a medicine the patient is currently prescribed. Every flag carries the rule, the table and the source that table came from, so a clinician can see whose guideline this is before acting on it. NOTHING IS PRE-LOADED. This product ships no gene-drug content at all: a table written from memory would be plausible, incomplete in ways nobody could see, and read as a reason to change somebody’s medicine, so what ships is the importer and an honest empty state, and the hospital loads the licensed table it uses. Hereditary cancer: a family with a hereditary cancer risk is kept as one record — the index patient’s gene, variant and classification as the laboratory reported them (linked to the filed report where there is one) beside every relative, whether they have been offered cascade testing, declined, been tested and what the laboratory found — so the family’s risk picture builds over years instead of living in a separate file for each relative. Genetics orders and interprets the tests; the app keeps the family’s status.

Who uses it: Built for: Oncology
Reads: Genetic reports the hospital files, active prescriptions, the loaded pharmacogenomic table
Writes: Reports, findings, the gene-drug flags computed from them, hereditary cancer families and cascade testing
Never: It does not sequence, interpret or reinterpret anything — the significance on every finding is the laboratory’s, typed off the laboratory’s report.
Access: Only people whose role includes it — the clinic owner decides who
Your data: Full PHI. Hosted in Boston, United States. On uninstall: Every record stays; only the workflow leaves.

In the product

Who uses it: Doctor — the demo profile it is best tried as
Where it opens: Clinical › Genetics /genomics
Permission: gene.read

Every clinical app in the handbook →

How it works

Load the pharmacogenomic tableUnder Reference table, name it, its version and where it came from, and paste the file with gene, phenotype, drug, effect and recommendation; evidence level is optional. Nothing ships pre-loaded. A load becomes the table in use and marks the previous one superseded, keeping its rules; reloading the same name and version replaces that table’s rules outright.
File a reportPatient, laboratory, report reference, the date it was reported, the panel and the laboratory’s summary in its own words.
Record each findingGene, variant, phenotype as the report states it, significance and what the laboratory wrote. A variant of uncertain significance carries no action — the service refuses one that does. For a hereditary cancer family, Hereditary cancer keeps the index result beside each relative’s cascade testing — offered, declined, tested and the result.
Read it against what the patient is takingA flag appears where a finding’s phenotype meets a rule in the current table and a medicine the patient is currently prescribed, naming the table, its version and its source. With no table loaded the panel says nothing is being checked, rather than showing a clean page.

Rules it keeps

What it does not do, by design. A listing with only benefits is an advertisement.

It does not sequence, interpret or reinterpret anything — the significance on every finding is the laboratory’s, typed off the laboratory’s report.

A variant of uncertain significance cannot carry an action: the database refuses the row, so “unknown” cannot quietly acquire an instruction.

It does not change a prescription; a flag is a row beside one.

And with no pharmacogenomic table loaded it produces no flags and says that nothing is being checked, rather than showing a clean page that reads like an all-clear.

AI in GeneLens

AskQuestions about what is on screen — “What needs attention in GeneLens today?” — answered with the records it read.

DraftSummaries and notes for the team, marked as drafts until a person signs.

Every answer shows its sources. Nothing AI writes is saved until a person accepts it.

See it on screen

GeneLens — Genetics — Read a genetic report against the medicines the patient takes — 01Genetics — Read a genetic report against the medicines the patient takesCaptured from the running demo clinic

01Genetics — Read a genetic report against the medicines the patient takesCaptured from the running demo clinic

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Connected to

Read out of the code, not the brochure: each app below is here because one service queries the other’s tables. Install either side and the hand-over is already wired.

Reads from · 2

Patient Registry RxCanvas

See the whole clinic →

Questions clinics ask

What does GeneLens do?

The genetic report, read against the medicines the patient is actually on — and a hereditary cancer family’s cascade testing. A genetic report arrives as a PDF and is filed. This puts it beside the prescription. The report is recorded as the laboratory issued it — its reference, its panel, and each finding in the laboratory’s own words — and the gene-drug flags are computed where three things meet: a finding that states a phenotype, a rule in the pharmacogenomic table this hospital has loaded, and a medicine the patient is currently prescribed. Every flag carries the rule, the table and the source that table came from, so a clinician can see whose guideline this is before acting on it. NOTHING IS PRE-LOADED. This product ships no gene-drug content at all: a table written from memory would be plausible, incomplete in ways nobody could see, and read as a reason to change somebody’s medicine, so what ships is the importer and an honest empty state, and the hospital loads the licensed table it uses. Hereditary cancer: a family with a hereditary cancer risk is kept as one record — the index patient’s gene, variant and classification as the laboratory reported them (linked to the filed report where there is one) beside every relative, whether they have been offered cascade testing, declined, been tested and what the laboratory found — so the family’s risk picture builds over years instead of living in a separate file for each relative. Genetics orders and interprets the tests; the app keeps the family’s status.

What data does GeneLens read and write?

GeneLens reads genetic reports the hospital files, active prescriptions, the loaded pharmacogenomic table and writes reports, findings, the gene-drug flags computed from them, hereditary cancer families and cascade testing. Its data class is Full PHI. Every app works on the same patient record — nothing is copied into a silo.

What does GeneLens deliberately not do?

It does not sequence, interpret or reinterpret anything — the significance on every finding is the laboratory’s, typed off the laboratory’s report. A variant of uncertain significance cannot carry an action: the database refuses the row, so “unknown” cannot quietly acquire an instruction. It does not change a prescription; a flag is a row beside one. And with no pharmacogenomic table loaded it produces no flags and says that nothing is being checked, rather than showing a clean page that reads like an all-clear.

What happens to our data if we uninstall GeneLens?

Every record stays; only the workflow leaves.

Is GeneLens available today?

Yes — GeneLens is live in clinics today. Set up your practice on MedAppz and install it from your dashboard.

Want to see GeneLens running on your own patients?

Tell us what you run and we will show you this app inside a practice shaped like yours — or answer the question the page above did not.

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