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) of 
+the [esm2_t6_8M_UR50D](https://huggingface.co/facebook/esm2_t6_8M_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 `80/20` train/test split. This model was trained with class weighting due to the imbalanced nature 
+of the RNA binding site dataset (fewer binding sites than non-binding sites). You can train your own version 
+using [this notebook](https://huggingface.co/AmelieSchreiber/esm2_t6_8M_weighted_lora_rna_binding/blob/main/LoRA_binding_sites_no_sweeps_v2.ipynb)!
 
+```
+{'eval_loss': 0.49476009607315063,
+'eval_precision': 0.14372964169381108,
+'eval_recall': 0.7526652452025586,
+'eval_f1': 0.24136752136752138,
+'eval_auc': 0.7710141129858947,
+'eval_runtime': 3.5601,
+'eval_samples_per_second': 9.27,
+'eval_steps_per_second': 2.528,
+'epoch': 15.0}
+```
+
+### 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_t6_8M_weighted_lora_rna_binding"
+# ESM2 base model
+base_model_path = "facebook/esm2_t6_8M_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]))
+
+```