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hy-0003/
MEDNA-DFM_6mA_XocBLS256

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MEDNA-DFM: A Dual-View FiLM-MoE Model for Explainable DNA Methylation Prediction

arXiv

This repository contains the official model weights and inference code for the paper: MEDNA-DFM: A Dual-View FiLM-MOE Model for Explainable DNA Methylation Prediction (He et al., 2026).

This specific repository hosts the fine-tuned model for predicting 6mA_Xoc BLS256.

📖 Paper Link: https://arxiv.org/abs/2602.22850

🚀 Quick Start (For Developers)

Due to specific architecture dependencies, please ensure you have transformers==4.18.0 installed. Run the following python script to dynamically download and run the model:

python

"""
Quick Start: MEDNA-DFM for DNA Methylation Prediction
This script demonstrates how to dynamically load the MEDNA-DFM model 
from the Hugging Face Hub and perform inference on raw DNA sequences.
"""

import sys
import torch
import requests
from huggingface_hub import snapshot_download


# Environment Patch for Legacy Dependencies
def patch_legacy_requests():
    """
    Patches the requests session to ensure compatibility between legacy 
    transformers (v4.18.0) and modern Hugging Face API endpoints.
    """
    original_request = requests.Session.request
    def patched_request(self, method, url, *args, **kwargs):
        if url.startswith('/api/'):
            # Route relative API paths through a stable mirror or hub URL
            url = 'https://hf-mirror.com' + url 
        return original_request(self, method, url, *args, **kwargs)
    requests.Session.request = patched_request


patch_legacy_requests()
print("Fetching MEDNA-DFM from Hugging Face Hub...")
REPO_ID = "hy-0003/MEDNA-DFM_6mA_XocBLS256"
cloud_model_path = snapshot_download(repo_id=REPO_ID)
sys.path.insert(0, cloud_model_path)
from configuration_medna import MednaConfig
from modeling_medna import MEDNADFMForSequenceClassification

print("Initializing model weights...")
model = MEDNADFMForSequenceClassification.from_pretrained(cloud_model_path)
model.eval()


# Inference on Sample DNA Sequences
# Typically, sequences centered around the target modification site (e.g., C or A)
test_sequences = [
    "CGCGCGCGCGCGCGCGCGCGCGCGCGCGCGCGCGCGCGCGC", # Sample 1: GC-rich motif
    "AAAAATTTTTAAAAATTTTTGAGGAAAAATTTTTAAAAATT"  # Sample 2: A-tract motif
]

with torch.no_grad():
    outputs = model(test_sequences)
    probabilities = torch.softmax(outputs.logits, dim=-1)


print(f"{'MEDNA-DFM Prediction Results':^50}")
for i, seq in enumerate(test_sequences):
    prob_0 = probabilities[i][0].item()
    prob_1 = probabilities[i][1].item()
    # Thresholding for binary classification
    prediction = "Methylated (1)" if prob_1 > 0.5 else "Unmethylated (0)"
    print(f"Sequence {i+1}:")
    print(f"  Snippet      : {seq[:10]} ... {seq[-10:]}")
    print(f"  P(Unmethylated) : {prob_0:.4f}")
    print(f"  P(Methylated)   : {prob_1:.4f}")
    print(f"  Prediction   : {prediction}")
    print("-" * 50)