Skip to content
cccskills
FreePublished on GitHub

evo2

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.

The English summary is being prepared. Showing the original description.

Works withHugging Face
See how to install

Files included (2)

  • SKILL.md5.3 KB
  • .catalog_stamp13 B

SKILL.md (original)

Review the instructions the agent will receive before you install.

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). Read compute_details({provider, mode:'read'}) for an environment with evo2 + flash-attn and a pre-cached HF weight mount, then submit:

c = host.compute.create(provider)
job = c.submitJob(
    intent="Evo2-7B score 200bp variant window — 1×GPU, ~2 min",
    inputs=[{"src": "score_evo2.py", "dstFilename": "score_evo2.py"}],
    command="python3 score_evo2.py",   # env selection is host-specific — see compute_details for your provider
    outputs=["scores.json"],
    timeoutSeconds=1800,
)
print(job.job_id)   # cell ends here — kernel never blocks on compute

Retain the exact returned job_id. Query that saved ID with the non-blocking c.attachJob(job_id).status() or .result() when its state or result is relevant; do not scan Job history. A final .result() read reports whether its follow-up was suppressed or had already been committed; otherwise the app starts the later analysis turn for an unread final result. See the remote-compute-ssh skill for details.

Inside score_evo2.py, point HF_HOME at the provider's weight-cache mount (path is in compute_details) and set HF_HUB_OFFLINE=1 so the loader doesn't 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.

Reviews

No reviews yet. Tell others what you thought.

Comments

No login needed. Share how it worked for you, ask a question, or note where it did not run.

No comments yet. Be the first to write one.

Comments are published right away. Do not include personal information such as email addresses or phone numbers. Up to 2 URLs.

0 / 1,000 characters

This form is protected by reCAPTCHA, and the Google Privacy Policy and Terms of Service apply.

More skills from this repository

Predict protein structure for monomers and multimers with AlphaFold2 via the ColabFold runner (Mirdita et al. 2022, github.com/sokrypton/ColabFold; AlphaFold2 Jumper et al. 2021). Reach for this skill to fold a sequence or complex with the AF2/AF2-Multimer evoformer, to validate designed sequences by self-consistency pLDDT, ipTM, and RMSD, or to run a quick MSA-backed prediction using the public MMseqs2 server.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

boltz

Free

Structure prediction for protein, nucleic-acid, and small-molecule complexes with Boltz-2 (Passaro & Wohlwend et al. 2025, github.com/jwohlwend/boltz). Reach for this skill to validate designed binders against a target, to co-fold a protein with a SMILES or CCD ligand, or to get an open-source AlphaFold3 alternative with optional binding-affinity prediction.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

borzoi

Free

Predict genome-wide functional tracks (RNA-seq, CAGE, DNase, ChIP) from DNA sequence with Borzoi. Use this skill when: (1) Scoring the regulatory effect of a variant on expression/accessibility, (2) Generating predicted coverage tracks for a locus, (3) Prioritising non-coding variants by predicted track delta.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

chai1

Free

Structure prediction for protein, nucleic-acid, and small-molecule complexes with the Chai-1 foundation model (Chai Discovery 2024, github.com/chaidiscovery/chai-lab). Reach for this skill to predict an antibody-antigen or protein-ligand complex from a single FASTA, to re-fold designed binders as an AlphaFold-multimer alternative, or to drive co-folding from Python for batched campaigns on a GPU.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

Prepare reproducible setup instructions and validate a user-managed named software environment on an Open-Science SSH Compute Host, including direct SSH and Slurm hosts. Use when a remote job needs packages, modules, cache variables, or a repeatable activation that the host does not already provide.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

Use when the user wants to create or manage a Specialist agent or create, revise, publish, or delete a Skill through the conversational `/Customize` entry. Routes Skill work to the internal skill-creator and handles Specialist work through the JavaScript host.agents SDK.

The English summary is being prepared. Showing the original description.

aipoch/open-science5.3KUpdated Oct 19, 2026

See all skills by aipoch

Report a problem with this skill