| name | ai-science-enformer-regulatory |
| description | Predict CAGE/DNase/ATAC/ChIP-seq tracks from raw DNA with Enformer/Borzoi, run in-silico mutagenesis (ISM), and score noncoding variant effects. Use when predicting enhancer/promoter activity from sequence, running ISM, scoring a noncoding SNP, or prioritizing GWAS/eQTL variants. |
| tool_type | python |
| primary_tool | enformer-pytorch |
Enformer: Regulatory Activity from DNA
When to Use
- Predicting CAGE/DNase/ATAC/ChIP-seq signal tracks directly from a raw DNA sequence (no alignment needed)
- Running in-silico mutagenesis (ISM) to find which bases in a promoter/enhancer drive a predicted track
- Scoring a noncoding SNP/indel for predicted effect on gene expression or chromatin accessibility
- Prioritizing GWAS/eQTL candidate variants by combining sequence-based effect size with population and functional evidence
- Needing RNA-seq/splicing-aware predictions over a larger (524 kb) window — use Borzoi instead of Enformer
Version Compatibility
enformer-pytorch >= 0.8 (PyTorch >= 2.0) — community PyTorch port of DeepMind's Enformer- Original TensorFlow weights via
tensorflow>=2.11 + tensorflow-hub (https://tfhub.dev/deepmind/enformer/1)
kipoiseq >= 0.7 for one-hot encoding / FASTA windowing utilities- Borzoi:
borzoi-pytorch (community port) or calico/borzoi (native, requires baskerville)
Prerequisites
pip install enformer-pytorch torch kipoiseq numpy (GPU strongly recommended: full forward pass is ~2 GB+ activations per sequence)- A reference genome FASTA (hg38 or mm10) to pull 196,608 bp windows from
- Familiarity with one-hot DNA encoding and BED-style genomic coordinates (see
bio-genome-intervals-bed-file-basics)
Key Facts
- Input: one-hot DNA, 196,608 bp x 4, centered on the region of interest
- Output: 896 bins x 128 bp (~114,688 bp predicted region) across 5,313 tracks (human) / 1,643 tracks (mouse) — CAGE, DNase, ATAC, ChIP-seq across 100+ cell types
- Architecture: stem conv -> 6 dilated conv blocks (progressive downsampling to 128 bp/bin) -> 11 transformer layers (8 heads, relative positional encodings) -> pointwise conv + softplus
- Training: Poisson log-likelihood loss against real -seq coverage, joint human (hg38) + mouse (mm10) heads
- Borzoi extends this to 524,288 bp input, 32 bp resolution, and adds RNA-seq coverage (captures splicing effects that Enformer's CAGE tracks miss)
Loading the Real Model and Running Inference
Goal: get raw track predictions for a 196,608 bp genomic window using the pretrained Enformer weights.
Approach: load the HuggingFace-hosted checkpoint via enformer-pytorch, one-hot encode a FASTA window with kipoiseq, and run a forward pass in eval mode.
import torch
from enformer_pytorch import Enformer, str_to_one_hot
def load_enformer(device: str = "cuda") -> Enformer:
"""Load the pretrained Enformer checkpoint from the HF Hub."""
model = Enformer.from_pretrained("EleutherAI/enformer-official-rough")
return model.to(device).eval()
def predict_tracks(model: Enformer, seq: str, device: str = "cuda"):
"""Run Enformer on a single 196,608 bp sequence.
Returns dict with 'human' -> (896, 5313) and 'mouse' -> (896, 1643) tensors.
seq must be exactly model.seq_length long (pad with 'N' if shorter).
"""
one_hot = str_to_one_hot(seq).unsqueeze(0).to(device)
with torch.no_grad():
out = model(one_hot, head="both" if hasattr(model, "heads") else None)
return out
In-Silico Mutagenesis (ISM)
Mutate one position at a time to the other 3 bases, re-run the model, and take the delta from baseline. This is the ground-truth way to attribute a track's signal to individual bases; it costs 3 * L forward passes so restrict pos to a small window (e.g. a candidate motif), not the whole 196 kb input.
import numpy as np
def mutate_base(seq: str, pos: int, alt: str) -> str:
"""Return seq with a single base substituted at pos."""
return seq[:pos] + alt + seq[pos + 1:]
def ism_scores(seq: str, pos: int, model_fn):
"""Compute per-allele ISM deltas at one position.
model_fn(seq) -> np.ndarray of track scores (already sliced to the track(s)
of interest, e.g. output['human'][:, bin_idx, track_idx].mean()).
Returns (ref_base, baseline_score, {alt_base: delta}).
"""
baseline = model_fn(seq)
ref = seq[pos]
effects = {}
for alt in "ACGT":
if alt == ref:
continue
effects[alt] = model_fn(mutate_base(seq, pos, alt)) - baseline
return ref, baseline, effects
Variant Scoring and Prioritization
Rank candidate variants by absolute predicted effect on the track(s) relevant to the phenotype (e.g. CAGE in the tissue of interest for eQTL follow-up). Combine the sequence-based score with orthogonal evidence — population allele frequency (gnomAD), GWAS/eQTL colocalization, and chromatin context — before calling a variant causal; a large ISM delta alone is not sufficient evidence.
def score_variant(seq: str, pos: int, alt: str, model_fn) -> float:
"""Predicted-track delta (mut - ref) for a single substitution at pos."""
base = model_fn(seq)
mut = model_fn(mutate_base(seq, pos, alt))
return float(mut - base)
def rank_variants(seq: str, candidates: list, model_fn) -> list:
"""candidates: list of (pos, alt) tuples. Returns sorted by |delta| desc,
each as (pos, ref_base, alt_base, delta)."""
scored = []
for pos, alt in candidates:
if alt == seq[pos]:
continue
d = score_variant(seq, pos, alt, model_fn)
scored.append((pos, seq[pos], alt, d))
return sorted(scored, key=lambda x: abs(x[3]), reverse=True)
def _toy_track_model(seq: str) -> float:
"""Cheap stand-in for model_fn during development/testing — counts a
TATA-box motif as a toy 'promoter activity' proxy so ISM/ranking logic
can be unit-tested without loading the real 250M-parameter model."""
return 0.4 + 0.25 * sum(1 for i in range(len(seq) - 5) if seq[i:i + 6] == "TATAAA")
if __name__ == "__main__":
test_seq = "A" * 120 + "TATAAA" + "A" * 120
ref, baseline, effects = ism_scores(test_seq, 122, _toy_track_model)
assert ref == "T"
assert all(d <= 0 for d in effects.values()), "disrupting TATAAA should not raise the toy score"
candidates = [(p, alt) for p in (118, 120, 122, 124, 126) for alt in "ACGT"]
ranked = rank_variants(test_seq, candidates, _toy_track_model)
assert ranked[0][0] in (120, 121, 122, 123, 124, 125), "top hit should fall inside the motif"
print("self-check passed:", ranked[:3])
Pitfalls
- 196 kb context, ~115 kb predicted: the outer flanks give the model context but are never scored — center your variant/motif of interest, don't put it near the edges
- ISM vs gradient attribution: ISM is exact but costs
O(3L) model calls; DeepLIFT/Integrated Gradients are cheaper but require access to model internals and can be noisier for saturated (softplus) outputs
- Track units are not linear "activity": outputs are Poisson-rate predictions (post-softplus) in log-ish space per 128 bp bin — compare deltas on the same track/bin, don't compare raw magnitudes across tracks
- Reference genome build: Enformer/Borzoi were trained on hg38/mm10 — pulling sequence from hg19 coordinates without a liftover will silently give wrong predictions
- The 11 transformer layers are what differentiate Enformer from conv-only baselines like Basenji2 — they are what let the model integrate signal across the full 100+ kb receptive field
- GPU memory: a single 196,608 bp forward pass holds large intermediate activations; batch size 1 on a 16 GB GPU is often the practical ceiling without mixed precision
See Also
ai-science-genomic-llms — sequence-only foundation models (DNA language models) as an alternative to track-supervised models like Enformerai-science-splicing-models — for splicing-specific effect prediction (SpliceAI etc.), complementary to Borzoi's RNA-seq headai-science-variant-to-structure-models — downstream structural consequence prediction once a variant is prioritizedbio-genome-intervals-bed-file-basics — coordinate handling for defining the input window
Sources
