How to use from the
Use from the
Transformers library
# Gated model: Login with a HF token with gated access permission
hf auth login
# Use a pipeline as a high-level helper
from transformers import pipeline

pipe = pipeline("text-generation", model="TaoMedAI/RareSeek-R1")
messages = [
    {"role": "user", "content": "Who are you?"},
]
pipe(messages)
# Load model directly
from transformers import AutoTokenizer, AutoModelForCausalLM

tokenizer = AutoTokenizer.from_pretrained("TaoMedAI/RareSeek-R1")
model = AutoModelForCausalLM.from_pretrained("TaoMedAI/RareSeek-R1")
messages = [
    {"role": "user", "content": "Who are you?"},
]
inputs = tokenizer.apply_chat_template(
	messages,
	add_generation_prompt=True,
	tokenize=True,
	return_dict=True,
	return_tensors="pt",
).to(model.device)

outputs = model.generate(**inputs, max_new_tokens=40)
print(tokenizer.decode(outputs[0][inputs["input_ids"].shape[-1]:]))
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RareSeek-R1: A specialized language model for rare disease diagnosis and reasoning

RareSeek-R1 is a domain-specialized large language model for rare-disease diagnostic reasoning, developed through a Progressive Parameter-Efficient Transfer Learning framework. The model is first instruction-tuned on the clinically grounded RareMed-Corpus, a large, multi-source dataset deeply integrated from medical textbooks, guidelines, biomedical literature, and real-world EHR narratives. It is then fine-tuned on RareMed-CoT, a high-fidelity corpus designed to instill explicit, stepwise clinical reasoning aligned with real diagnostic workflows. To further enhance factual reliability, GraphRAG is incorporated to anchor the model’s inference to up-to-date variant–gene–phenotype–disease relationships. This retrieval augmentation substantially reduces hallucinations, improves factual calibration, and yields notable performance gains—particularly when EHR narratives are combined with prioritized genetic variants. Together, RareSeek-R1 performs direct reasoning over full-length EHRs, leverages graph-grounded retrieval, and demonstrably augments clinician-level diagnostic accuracy, advancing a reliable and scalable AI paradigm for rare-disease diagnosis.

RareSeek-R1 Teaser Image

RareMedData: https://huggingface.co/datasets/TaoMedAI/RareMedData

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