genomic-intelligence
Predict regulatory features, gene structure, and expression directly from DNA sequence using Genomic Intelligence's hosted transformer DNA language models — no local GPU or model weights. Six tasks over a REST API and a hosted MCP server (keyless public demo): promoter regions, splice donor/acceptor sites, enhancer activity, chromatin state, sequence-to-expression (log TPM), and de-novo gene annotation, plus a composite find-genes-then-predict-expression workflow. Use when the user has a gene symbol, a genomic region, or a DNA/FASTA sequence and wants any of these predictions, mentions Genomic Intelligence, genomicintelligence.ai, api.genomicintelligence.ai, or mcp.genomicintelligence.ai.
git clone --depth 1 https://github.com/K-Dense-AI/scientific-agent-skills /tmp/genomic-intelligence && cp -r /tmp/genomic-intelligence/skills/genomic-intelligence ~/.claude/skills/genomic-intelligenceSKILL.md
# Genomic Intelligence — DNA Sequence Models
Genomic Intelligence (GI) serves transformer DNA language models over six
sequence-analysis tasks on managed GPUs. Give it a **gene symbol**, a **genomic
region**, or a **DNA/FASTA sequence**; it returns structured predictions —
promoter regions, splice sites, enhancer activity, chromatin state, expression
(log TPM), and de-novo gene annotation. Nothing runs locally: no model weights,
no GPU, no heavy Python stack. It is a thin client over a hosted, versioned
inference API.
**Official docs:** [docs.genomicintelligence.ai](https://docs.genomicintelligence.ai) ·
REST contract at [api.genomicintelligence.ai/v1/openapi.json](https://api.genomicintelligence.ai/v1/openapi.json) ·
hosted MCP server at `https://mcp.genomicintelligence.ai/mcp`
## When to use this skill
Use GI when the user has DNA and wants a model prediction:
- **Find promoters** in a genomic region (`promoter`)
- **Predict splice** donor/acceptor sites (`splice`)
- **Score enhancer activity** — developmental & housekeeping (`enhancer`)
- **Annotate chromatin state** across hundreds of tracks (`chromatin`)
- **Predict expression** as log(TPM+1) from a sequence + cell-type context (`expression`)
- **Annotate genes/transcripts** de novo, no reference needed (`annotation`)
- **Find the genes in a region and predict each one's expression** (composite)
Not for local alignment, variant calling, or file I/O — use a local tool
(BioPython, bcftools) for those. GI is for **model inference from sequence**.
> For research and development use, **not clinical or diagnostic decisions**.
## Two ways to call GI
### Hosted MCP server (best for AI agents — keyless)
GI hosts an MCP server at `https://mcp.genomicintelligence.ai/mcp` (Streamable
HTTP). When your agent host supports MCP, prefer it: it works **keyless** against
a capped public demo quota (zero setup), and an optional `gi_` bearer key raises
the quota. It exposes acquisition tools that return a **sequence handle**
(`sequence_ref`) and `predict_*` tools that take that handle — so large sequences
never bloat the context. See [MCP workflow](#mcp-workflow-handle-based) below and
`references/mcp.md`.
### REST API (universal)
Plain HTTP with `requests` against `https://api.genomicintelligence.ai/v1`. The
REST path **requires** a `GI_API_KEY` (a `gi_` bearer). Use it on any host, in
scripts, or when you need the raw envelope. See [Core REST workflow](#core-rest-workflow).
## Access and authentication
1. The **hosted MCP demo is keyless** — try it with nothing set.
2. The **REST `/v1` API needs a key**, sent as `Authorization: Bearer <key>`.
Request one at [contact@genomicintelligence.ai](mailto:contact@genomicintelligence.ai).
3. **Never hardcode the key.** Read it from the `GI_API_KEY` environment variable
(or a `.env` via `python-dotenv`). Never commit keys.
```bash
export GI_API_KEY="gi_yourkeyhere" # optional for MCP; required for REST
export GI_BASE_URL="https://api.genomicintelligence.ai" # override for staging
```
Keys are scoped to a partner tier with concurrency and per-minute caps. A `429`
means you hit a cap — back off and retry, or ask GI to raise your tier.
## The six tasks
All REST tasks share one shape: `POST /v1/tasks/{task}/predict` with body
`{sequence, sequence_name, model?, options?}`, returning a `{data, meta}`
envelope. What differs per task:
| Task | Mode | Length bound | Notes |
|---|---|---|---|
| `promoter` | sync | 1–500,000 bp | sliding-window promoter regions |
| `splice` | sync | 1–500,000 bp | donor/acceptor sites (long-context BigBird) |
| `enhancer` | sync | 1–500,000 bp | dev + housekeeping scores (DeepSTARR, *Drosophila*) |
| `chromatin` | sync | 1–500,000 bp | hundreds of tracks (DeepSEA) |
| `expression` | sync | **exactly 9,198 bp** | log(TPM+1); needs a cell-type `description` |
| `annotation` | **async** | 1–500,000 bp | de-novo transcripts; submit + poll |
**Omit `model` and the API uses the task's default** — that is the recommended
call. Default model IDs are intentionally **not** documented here: defaults
change and retired IDs fail hard, so never hardcode one. To pin a model, or to
pick a non-human one (Drosophila, yeast, and Arabidopsis models exist for several
tasks), discover IDs at call time with `GET /v1/tasks/{task}/models` (REST) or
`list_models` (MCP) — and **never invent one**. Full per-task output shapes are
in `references/tasks.md`.
Two hard rules the model enforces:
- **`expression` needs exactly 9,198 bp**, a window **centred on the TSS**
(4,599 upstream + TSS + 4,598 downstream). Any other length is rejected. Use the acquisition helpers below to
build it — do not truncate by hand.
- **`expression` needs a `description`** — a cell-type / assay string (e.g.
`"K562 cells"`), passed as `options.description`.
## Sequence acquisition
You rarely start from a raw 9,198 bp string. Acquire sequence first:
- **From a gene symbol** → MCP `fetch_ensembl_sequence(gene=...)`; **from
coordinates** → `fetch_region(region=...)`. Both fetch public Ensembl reference
sequence (no key). REST users can query Ensembl REST directly. (`find_genes` is
the annotation task, not an acquisition tool.)
- **For `expression`** → use the TSS-centred fetch so the window is exactly
9,198 bp. MCP: `fetch_gene_for_expression` (handles the centring). Do not
build the window by hand.
- **From a local FASTA** → MCP `store_inline_sequence`, or read the file yourself
for REST. (`load_local_fasta` exists only in local deployments, not on the
hosted server.)
- **A demo sequence** → MCP `load_demo_sequence(name=...)` returns a ready handle
(great for a keyless smoke test); `name` is required.
See `references/sequence-acquisition.md` for the exact Ensembl calls and the
expression-window math.
## Core REST workflow
Sync tasks (promoter, splice, enhancer, chromatin, expression) are one call:
```python
import os, requests
BASE = os.environ.get("GI_BASE_URL", "https://api.genomiHow to use the Adaptyv Bio Foundry API and Python SDK for protein experiment design, submission, and results retrieval. Use this skill whenever the user mentions Adaptyv, Foundry API, protein binding assays, protein screening experiments, BLI/SPR assays, thermostability assays, or wants to submit protein sequences for experimental characterization. Also trigger when code imports `adaptyv`, `adaptyv_sdk`, or `FoundryClient`, or references `foundry-api-public.adaptyvbio.com`.
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