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Esm

biotender-max/esm

> ESM2 protein language model for embeddings and sequence scoring. (2) Getting protein embeddings for clustering, (3) Filtering designs by sequence plausibility, (4) Zero-shot variant effect prediction, (5) Analyzing sequence-function relationships. For structure prediction, use chai or boltz. For QC thresholds, use protein-qc.

1k tokens
context cost
the whole folder, loaded on every use
1
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instructions only
0
copies elsewhere
how many repositories repackaged it
132
stars on the repo
on the repository, not the skill itself

Install

one command, takes just this skill from the repository
npx skills add https://github.com/BioTender-max/awesome-bio-agent-skills --skill esm

The instruction itself

16 sections, as written by the author

ESM2 Protein Language Model

Prerequisites

| Requirement | Minimum | Recommended |

|-------------|---------|-------------|

| Python | 3.8+ | 3.10 |

| PyTorch | 1.10+ | 2.0+ |

| CUDA | 11.0+ | 11.7+ |

| GPU VRAM | 8GB | 24GB (A10G) |

| RAM | 16GB | 32GB |

How to run

> First time? See Installation Guide to set up Modal and biomodals.

Option 1: Modal

cd biomodals
modal run modal_esm2_predict_masked.py \
  --input-faa sequences.fasta \
  --out-dir embeddings/

GPU: A10G (24GB) | Timeout: 300s default

import torch
import esm

# Load model
model, alphabet = esm.pretrained.esm2_t33_650M_UR50D()
batch_converter = alphabet.get_batch_converter()
model = model.eval().cuda()

# Process sequences
data = [("seq1", "MKTAYIAKQRQISFVK...")]
batch_labels, batch_strs, batch_tokens = batch_converter(data)

with torch.no_grad():
    results = model(batch_tokens.cuda(), repr_layers=[33])

# Get embeddings
embeddings = results["representations"][33]

Key parameters

ESM2 Models

| Model | Parameters | Speed | Quality |

|-------|------------|-------|---------|

| esm2_t6_8M | 8M | Fastest | Fast screening |

| esm2_t12_35M | 35M | Fast | Good |

| esm2_t33_650M | 650M | Medium | Better |

| esm2_t36_3B | 3B | Slow | Best |

Output format

embeddings/
├── embeddings.npy       # (N, 1280) array
├── pll_scores.csv       # PLL for each sequence
└── metadata.json        # Sequence info

Sample output

Successful run

$ modal run modal_esm2_predict_masked.py --input-faa designs.fasta
[INFO] Loading ESM2-650M model...
[INFO] Processing 100 sequences...
[INFO] Computing pseudo-log-likelihood...

embeddings/pll_scores.csv:
sequence_id,pll,pll_normalized,length
design_0,-0.82,0.15,78
design_1,-0.95,0.08,85
design_2,-1.23,-0.12,72
...

Summary:
  Mean PLL: -0.91
  Sequences with PLL > 0: 42/100 (42%)

What good output looks like:

  • PLL_normalized: > 0.0 (more natural-like)
  • Embeddings shape: (N, 1280) for 650M model
  • Higher PLL = more natural sequence

Decision tree

Should I use ESM2?
│
├─ What do you need?
│  ├─ Sequence plausibility score → ESM2 PLL ✓
│  ├─ Embeddings for clustering → ESM2 ✓
│  ├─ Variant effect prediction → ESM2 ✓
│  └─ Structure prediction → Use ESMFold
│
├─ What model size?
│  ├─ Fast screening → esm2_t12_35M
│  ├─ Standard use → esm2_t33_650M ✓
│  └─ Best quality → esm2_t36_3B
│
└─ Use case?
   ├─ QC filtering → PLL > 0.0 threshold
   ├─ Diversity analysis → Mean-pooled embeddings
   └─ Mutation scanning → Per-position log-odds

PLL interpretation

| Normalized PLL | Interpretation |

|----------------|----------------|

| > 0.2 | Very natural sequence |

| 0.0 - 0.2 | Good, natural-like |

| -0.5 - 0.0 | Acceptable |

| < -0.5 | May be unnatural |

Typical performance

| Campaign Size | Time (A10G) | Cost (Modal) | Notes |

|---------------|-------------|--------------|-------|

| 100 sequences | 5-10 min | ~$1 | Quick screen |

| 1000 sequences | 30-60 min | ~$5 | Standard |

| 5000 sequences | 2-3h | ~$20 | Large batch |

Throughput: ~100-200 sequences/minute with 650M model.


Verify

wc -l embeddings/pll_scores.csv  # Should match input + 1 (header)

Troubleshooting

OOM errors: Use smaller model or batch sequences

Slow processing: Use esm2_t12_35M for speed

Low PLL scores: May indicate unusual/designed sequences

Error interpretation

| Error | Cause | Fix |

|-------|-------|-----|

| RuntimeError: CUDA out of memory | Sequence too long or large batch | Reduce batch size |

| KeyError: representation | Wrong layer requested | Use layer 33 for 650M model |

| ValueError: sequence | Invalid amino acid | Check for non-standard AAs |


Next: Structure prediction with chai or boltzprotein-qc for filtering.

How to use it

Copy the folder

Take biotender-max/esm from the repository into ~/.claude/skills for personal use, or into .claude/skills inside a project.

Check the name does not clash

The agent identifies a skill by the name field in its header. Two skills with the same name cannot sit side by side — one of them will be ignored.