Evo2
Open-source, local-first desktop AI research workbench for scientific computing with Python/R, MCP bioinformatics tools, SSH/WSL/GPU runtimes, and OpenAI/Anthropic models.
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What its author says it does
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Score, embed, and generate DNA sequences with Evo 2, a long-context genomic foundation model. Use this skill when: (1) Computing per-nucleotide or per-sequence likelihoods for variant effect scoring, (2) Embedding genomic windows for downstream classification, (3) Generating DNA conditioned on a prefix, (4) Scoring regulatory or coding regions across species.
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SKILL.md
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Evo 2 — DNA Language Model
Prerequisites
| Requirement | Minimum | Recommended |
|---|---|---|
| Python | 3.11 | 3.12 (<3.13) |
| CUDA | 12.1+ | 12.4+ |
| GPU VRAM | 24 GB (7B bf16) | 80 GB (40B) |
| RAM | 32 GB | 128 GB |
How to run
Installation
pip install evo2
# Weights pulled from Hugging Face on first model load.
Loading and scoring
from evo2 import Evo2
model = Evo2("evo2_7b") # or "evo2_40b" — see model table
seqs = ["ATCG" * 50, "GGGCTTAA" * 25]
ll = model.score_sequences(seqs) # → list[float], mean per-token log-likelihood
print(ll)
Generation
out = model.generate(
prompt_seqs=["ATGAAAGCT"],
n_tokens=256,
temperature=0.7,
)
print(out.sequences[0])
Models
| Name | Params | Context | VRAM (bf16) | Notes |
|---|---|---|---|---|
evo2_7b | 7 B | 1 M nt | ~22 GB | Default; fits on a single 24 GB+ GPU |
evo2_40b | 40 B | 1 M nt | ~78 GB | H100 80 GB or multi-GPU |
evo2_1b_base | 1 B | 8 K nt | ~6 GB | FP8 path requires sm_89+ (H100) |
Output format
score_sequences returns a list[float] (or np.ndarray) of mean log-likelihoods,
one per input sequence. More negative ⇒ less likely under the model. For variant
effect, compute Δll = ll_alt - ll_ref over a fixed window.
generate returns a GenerationOutput with .sequences (list[str]), .logits
(list[Tensor]), and .logprobs_mean (list[float]) — always populated, no flag required.
Decision tree
Need a DNA model?
│
├─ Per-base/per-sequence likelihood, generation → Evo 2 ✓
├─ Predict experimental tracks (expression, accessibility) → borzoi
└─ Protein, not DNA → fair-esm2 / esmfold2
Remote compute
7B/40B inference is GPU-bound (≥24 GB / 80 GB VRAM). Use a selected and
probed ssh:<alias> context and load remote-compute-ssh. Confirm that the
environment imports Evo 2 and that the desired weights are cached. Submit a
self-contained scoring script through one run_in_context call:
{
"context_id": "ssh:gpu-box",
"title": "Evo 2 variant scoring",
"command": "source ~/miniforge3/etc/profile.d/conda.sh && conda activate evo2 && HF_HOME=/srv/model-cache HF_HUB_OFFLINE=1 python score_evo2.py --output /home/me/wisp-results/evo2/scores.json",
"timeout_secs": 1800,
"input_paths": ["runs/score_evo2.py"],
"output_specs": [
{
"glob": "ssh://gpu-box/home/me/wisp-results/evo2/scores.json",
"kind": "json",
"residency": "remote"
}
]
}
Replace context, environment, cache, and output paths with discovered values.
Call monitor_run once to wait, get_run once for a snapshot, or cancel_run
to stop. Set HF_HUB_OFFLINE=1 only after confirming the cache is complete, so
the loader does not try to write refs/ into a read-only mount. Weight footprint:
~15 GB (7B), ~80 GB (40B).
Typical performance
| Task | 7B on H100 | Notes |
|---|---|---|
| Model load (cached) | ~5-7 min | First call hydrates weights |
score_sequences, 200×200bp | ~10-20 s | After load |
generate, 1×512 nt | ~15 s |
Troubleshooting
| Symptom | Cause | Fix |
|---|---|---|
Transformer Engine not installed | No FP8 — falls back to bf16 | Informational only on non-H100; ignore |
| OOM on load | 40B on <80 GB GPU | Use evo2_7b or shard with device_map |
HF tries to write refs/main | HF_HOME points at RO mount | Set HF_HUB_OFFLINE=1 |
dtype mismatch in score_sequences | Passing tensors not strings | Pass list[str]; the API tokenises for you |
Next: pair with borzoi to predict track-level effects of the same
variants.