---
library_name: transformers
tags: []
---

# Model Card for Model ID

<!-- Provide a quick summary of what the model is/does. -->
Finetuned "BioMistral/BioMistral-7B" with MedQA dataset. 

## Model Details
A Collection of Open-Source Pretrained Large Language Models for Medical Domains finetuned with MedQA dataset.

### Model Description

<!-- Provide a longer summary of what this model is. -->

This is the model card of a 🤗 transformers model that has been pushed on the Hub. This model card has been automatically generated.

- **Developed by:** mychen76
- **Model type:** BioMedical
- **Finetuned from model:** BioMistral/BioMistral-7B

### Model Sources [optional]

<!-- Provide the basic links for the model. -->
- **dataset:** MedQA dataset

 
## How to Get Started with the Model

Use the code below to get started with the model.
<!-- Address questions around how the model is intended to be used, including the foreseeable users of the model and those affected by the model. -->
Load Model:
```python
import torch
from transformers import AutoTokenizer, AutoModelForCausalLM, BitsAndBytesConfig

base_model_id = "mychen76/biomistral_medqa_v1"
bnb_config = BitsAndBytesConfig(
    load_in_4bit=True,
    bnb_4bit_use_double_quant=True,
    bnb_4bit_quant_type="nf4",
    bnb_4bit_compute_dtype=torch.bfloat16
)

model = AutoModelForCausalLM.from_pretrained(base_model_id, quantization_config=bnb_config)
tokenizer = AutoTokenizer.from_pretrained(
    base_model_id,
    add_eos_token=True,
    add_bos_token=True,
)

## Uses

```
*** Information ***
```
eval_prompt = """From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
information

### Question:
What are the genetic changes related to X-linked lymphoproliferative disease ?

### Answer:
"""

model_input = eval_tokenizer(eval_prompt, return_tensors="pt").to("cuda")

ft_model.eval()
with torch.no_grad():
    print(eval_tokenizer.decode(ft_model.generate(**model_input, max_new_tokens=300)[0], skip_special_tokens=True))
```
result:
```
From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
information

### Question:
What are the genetic changes related to X-linked lymphoproliferative disease ?

### Answer:
X-linked lymphoproliferative disease (XLP) is a rare primary immunodeficiency syndrome. XLP is caused by mutations in SH2D1A gene, which encodes the cytoplasmic signaling protein SLAM-associated protein ( client protein-SLAM). SLAM is a member of the signaling lymphocytic activation molecule family of receptors, which are involved in the regulation of lymphocyte activation and proliferation. The SLAM receptor is expressed on the surface of B and T lymphocytes, natural killer cells, and monocytes. Mutations in SH2D1A gene lead to impaired signaling through the SLAM receptor, resulting in a deficiency in the activation and proliferation of B and T lymphocytes. This leads to a decrease in the number of B and T lymphocytes, resulting in a weakened immune response.
```

*** Frequency ***
```
eval_prompt = """From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
frequency

### Question:
How many people are affected by Smith-Lemli-Opitz syndrome ?

### Answer:
"""

model_input = eval_tokenizer(eval_prompt, return_tensors="pt").to("cuda")

ft_model.eval()
with torch.no_grad():
    print(eval_tokenizer.decode(ft_model.generate(**model_input, max_new_tokens=300)[0], skip_special_tokens=True))
```
result:
```
From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
frequency

### Question:
How many people are affected by Smith-Lemli-Opitz syndrome ?

### Answer:
Smith-Lemli-Opitz syndrome (SLOS) is a rare autosomal recessive disorder of human development. It is characterized by a wide range of symptoms, including growth and developmental delay, intellectual disability, characteristic facial features, and congenital heart defects. The prevalence of SLOS is estimated to be 1 in 15,000 to 1 in 25,000 live births.
```

*** Symptons ***
```
eval_prompt = """From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
symptoms

### Question:
What are the symptoms of Norrie disease ?

### Answer:
"""

model_input = eval_tokenizer(eval_prompt, return_tensors="pt").to("cuda")

ft_model.eval()
with torch.no_grad():
    print(eval_tokenizer.decode(ft_model.generate(**model_input, max_new_tokens=300)[0], skip_special_tokens=True))
```
Result:
```
Setting `pad_token_id` to `eos_token_id`:2 for open-end generation.

From the MedQuad MedicalQA Dataset: Given the following medical question and question type, provide an accurate answer:

### Question type:
symptoms

### Question:
What are the symptoms of Norrie disease ?

### Answer:
Norrie disease is a rare, X-linked recessive disorder of the blood vessels. It is characterized by a variety of symptoms, including glaucoma, mental retardation, seizures, and deafness.
```


### Out-of-Scope Use

images
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[More Information Needed]

## Bias, Risks, and Limitations

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[More Information Needed]

### Recommendations

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Users (both direct and downstream) should be made aware of the risks, biases and limitations of the model. More information needed for further recommendations.


[More Information Needed]

## Training Details

### Training Data

- **dataset:** keivalya/MedQuad-MedicalQnADataset
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[More Information Needed]

### Training Procedure

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## Citation

Arxiv : https://arxiv.org/abs/2402.10373

@misc{labrak2024biomistral,
      title={BioMistral: A Collection of Open-Source Pretrained Large Language Models for Medical Domains}, 
      author={Yanis Labrak and Adrien Bazoge and Emmanuel Morin and Pierre-Antoine Gourraud and Mickael Rouvier and Richard Dufour},
      year={2024},
      eprint={2402.10373},
      archivePrefix={arXiv},
      primaryClass={cs.CL}
}