Instructions to use medarc/H-optimus-0-SPECTRA with libraries, inference providers, notebooks, and local apps. Follow these links to get started.
- Libraries
- timm
How to use medarc/H-optimus-0-SPECTRA with timm:
import timm model = timm.create_model("hf-hub:medarc/H-optimus-0-SPECTRA", pretrained=True) - Notebooks
- Google Colab
- Kaggle
H-optimus-0-SPECTRA
MedARC · Sophont · Paper (coming soon)
H-optimus-0-SPECTRA is H-optimus-0 adapted with SPECTRA by MedARC and Sophont. We trained on registered PLISM image tiles, aligning representations of the same tissue across scanners and stains with a contrastive objective. The learned updates are merged into the full model weights.
The model maps RGB histology tiles to 1,536-dimensional embeddings for downstream analysis. All inference weights are included; no separate base checkpoint, adapter, or cluster access is required.
Inference
In a Python environment:
uv pip install torch torchvision "timm==1.0.30" huggingface_hub safetensors pillow
import torch
import timm
from PIL import Image
from timm.data import create_transform, resolve_model_data_config
device = "cuda" # Use "cpu" to run without a GPU.
model = timm.create_model(
"hf-hub:medarc/H-optimus-0-SPECTRA", pretrained=True,
).eval().to(device)
transform = create_transform(**resolve_model_data_config(model), is_training=False)
image = Image.open("tile.png").convert("RGB")
batch = transform(image).unsqueeze(0).to(device)
with torch.inference_mode():
tokens = model.forward_features(batch)
embedding = tokens[:, 0]
print(embedding.shape) # torch.Size([1, 1536])
The configuration supplies bicubic resizing to 256 pixels, a 224 × 224 center crop, and H&E-specific normalization stored in config.json. The embedding uses the CLS token. Use tissue tiles sampled at 0.5 µm/pixel, following the base model.
These are tile embeddings. Slide-level predictions require a downstream model.
Paper
Coming soon. We will add the paper link and citation here.
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