Update README.md

README.md

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 ---
 library_name: peft
+license: mit
+language:
+- en
+tags:
+- transformers
+- biology
+- esm
+- esm2
+- protein
+- protein language model
 ---
+# ESM-2 RNA Binding Site LoRA
+
+This is a Parameter Efficient Fine Tuning (PEFT) Low Rank Adaptation ([LoRA](https://huggingface.co/docs/peft/task_guides/token-classification-lora)) of 
+the [esm2_t12_35M_UR50D](https://huggingface.co/facebook/esm2_t12_35M_UR50D) model for the (binary) token classification task of 
+predicting RNA binding sites of proteins. The Github with the training script and conda env YAML can be
+[found here](https://github.com/Amelie-Schreiber/esm2_LoRA_binding_sites/tree/main). You can also find a version of this model 
+that was fine-tuned without LoRA [here](https://huggingface.co/AmelieSchreiber/esm2_t6_8M_UR50D_rna_binding_site_predictor). 
+
 ## Training procedure
 
-### Framework versions
+This is a Low Rank Adaptation (LoRA) of `esm2_t6_8M_UR50D`, 
+trained on `166` protein sequences in the [RNA binding sites dataset](https://huggingface.co/datasets/AmelieSchreiber/data_of_protein-rna_binding_sites)
+using a `75/25` train/test split. It achieves an evaluation loss of `0.18801096081733704`. 
 
+### Framework versions
 
 - PEFT 0.4.0
+
+## Using the Model
+
+To use, try running:
+```python
+from transformers import AutoModelForTokenClassification, AutoTokenizer
+from peft import PeftModel
+import torch
+
+# Path to the saved LoRA model
+model_path = "AmelieSchreiber/esm2_t30_150M_LoRA_RNA_binding"
+# ESM2 base model
+base_model_path = "facebook/esm2_t30_150M_UR50D"
+
+# Load the model
+base_model = AutoModelForTokenClassification.from_pretrained(base_model_path)
+loaded_model = PeftModel.from_pretrained(base_model, model_path)
+
+# Ensure the model is in evaluation mode
+loaded_model.eval()
+
+# Load the tokenizer
+loaded_tokenizer = AutoTokenizer.from_pretrained(base_model_path)
+
+# Protein sequence for inference
+protein_sequence = "MAVPETRPNHTIYINNLNEKIKKDELKKSLHAIFSRFGQILDILVSRSLKMRGQAFVIFKEVSSATNALRSMQGFPFYDKPMRIQYAKTDSDIIAKMKGT"  # Replace with your actual sequence
+
+# Tokenize the sequence
+inputs = loaded_tokenizer(protein_sequence, return_tensors="pt", truncation=True, max_length=1024, padding='max_length')
+
+# Run the model
+with torch.no_grad():
+    logits = loaded_model(**inputs).logits
+
+# Get predictions
+tokens = loaded_tokenizer.convert_ids_to_tokens(inputs["input_ids"][0])  # Convert input ids back to tokens
+predictions = torch.argmax(logits, dim=2)
+
+# Define labels
+id2label = {
+    0: "No binding site",
+    1: "Binding site"
+}
+
+# Print the predicted labels for each token
+for token, prediction in zip(tokens, predictions[0].numpy()):
+    if token not in ['<pad>', '<cls>', '<eos>']:
+        print((token, id2label[prediction]))
+
+```
+