The first MCP server
for your DNA.
Point Claude at your DNA. Ask in English.
$ claude mcp add lifecodecAsk questions no API can answer.
questionanswer
When should I schedule deep work?
Your variants and your actual sleep both put your peak window at 10am–1pm. You've booked 60% of your meetings inside it.
Why do two drinks wreck me?
You carry a reduced-activity ALDH2 variant, so acetaldehyde clears slowly. The flush and the headache are the same cause.
Should I bother with lactose-free?
No. rs4988235 is T/T — you're lactase persistent. Whatever dairy does to you, it isn't the lactose.
You don’t call these. Your agent does.
It lists the tools the moment it connects and picks whichever one your question needs. Reach for the SDK when you want types and retries, or go straight at the endpoints.
lifecode_get_variants({ gene: "CYP1A2" })calling…Your gadgets change. Your genome doesn’t.
You’ll swap watches three times this decade and lose the history each time. Build on the one input that’s still the same file in 2050.
Sequenced once, re-read by whatever model is best that year.
100 gigabytes in. Two kilobytes out.
Your genome will never fit in a context window, and it shouldn't have to. Finding the one locus that answers the question is the work.
3.1 billion bases · chr15:75,041,185 is the one we needed
{ "rsid": "rs762551", "gene": "CYP1A2", "genotype": "A/C", "effect": "reduced inducibility", "depth": 34.2 }
that’s 0.000002% of the file — the other 99.999998% is why this is a service and not a download
You can’t rotate your genome.
You can roll a key, change a password, get a new card number. Not this — and it partly describes your family too.
So an agent gets the narrowest thing that answers the question. Raw access is its own scope, off unless someone deliberately grants it, and revoking actually revokes. We never see your prompts — tool calls reach us, the conversation doesn’t.
Claude · access token
lc_tok_8f3a…d21cexpires
14:52
variants:readGenotypes at specific genestraits:readComputed traits and directionscoverage:readRead depth, so it can judge confidenceraw:downloadYour raw VCF, whole. Signed links, 15 minutes.
Bring your own genome.
One swab, read at clinical depth, yours for life. Then point whatever you’re building at it.