How to use from the
Use from the
Transformers library
# 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", device_map="auto")
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]:]))
Quick Links

🧬 RareSeek-R1

A Specialized Language Model for Rare Disease Diagnosis and Clinical Reasoning

📖 Model Overview

RareSeek-R1 is a domain-specialized large language model tailored 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 (Electronic Health Record) narratives. It is subsequently fine-tuned on RareMed-CoT, a high-fidelity corpus designed to instill explicit, stepwise clinical reasoning that aligns with real-world diagnostic workflows.

Figure 1: Overall framework and pipeline of RareSeek-R1. Figure 1: Overall framework and pipeline of RareSeek-R1.

🗄️ Dataset & Resources

📚 RareMedData: Access the comprehensive medical dataset used for training here:
👉 https://huggingface.co/datasets/TaoMedAI/RareMedData

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