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Evo2

Skill xuzhougeng/wisp-science/skills/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.

Install
npx -y skills add xuzhougeng/wisp-science --skill evo2

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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

RequirementMinimumRecommended
Python3.113.12 (<3.13)
CUDA12.1+12.4+
GPU VRAM24 GB (7B bf16)80 GB (40B)
RAM32 GB128 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

NameParamsContextVRAM (bf16)Notes
evo2_7b7 B1 M nt~22 GBDefault; fits on a single 24 GB+ GPU
evo2_40b40 B1 M nt~78 GBH100 80 GB or multi-GPU
evo2_1b_base1 B8 K nt~6 GBFP8 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

Task7B on H100Notes
Model load (cached)~5-7 minFirst call hydrates weights
score_sequences, 200×200bp~10-20 sAfter load
generate, 1×512 nt~15 s

Troubleshooting

SymptomCauseFix
Transformer Engine not installedNo FP8 — falls back to bf16Informational only on non-H100; ignore
OOM on load40B on <80 GB GPUUse evo2_7b or shard with device_map
HF tries to write refs/mainHF_HOME points at RO mountSet HF_HUB_OFFLINE=1
dtype mismatch in score_sequencesPassing tensors not stringsPass list[str]; the API tokenises for you

Next: pair with borzoi to predict track-level effects of the same variants.

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