added app file
Browse files
app.py
ADDED
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| 1 |
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import streamlit as st
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| 2 |
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from transformers import AutoTokenizer, AutoModelForSequenceClassification
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import torch
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import pandas as pd
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import plotly.express as px
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# Sequence splitting function
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def split_sequence(sequence, max_len=1024, overlap=512):
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chunks = []
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for i in range(0, len(sequence), max_len - overlap):
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chunk = sequence[i:i + max_len]
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if len(chunk) > 0:
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chunks.append(chunk)
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return chunks
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# Load model and tokenizer
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@st.cache_resource
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def load_model_and_tokenizer(model_name):
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model = AutoModelForSequenceClassification.from_pretrained(
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model_name, ignore_mismatched_sizes=True, trust_remote_code=True
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)
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tokenizer = AutoTokenizer.from_pretrained(model_name)
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return model, tokenizer
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def predict_chunk(model, tokenizer, chunk):
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tokens = tokenizer(chunk, return_tensors="pt", truncation=True, padding=True)
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with torch.no_grad():
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outputs = model(**tokens)
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return outputs.logits
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def nucArg_app():
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# Class mappings
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long_read_classes = {
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0: 'aminoglycoside', 1: 'bacitracin', 2: 'beta_lactam', 3: 'chloramphenicol',
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4: 'fosfomycin', 5: 'fosmidomycin', 6: 'fusidic_acid', 7: 'glycopeptide',
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8: 'kasugamycin', 9: 'macrolide-lincosamide-streptogramin', 10: 'multidrug',
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11: 'mupirocin', 12: 'non_resistant', 13: 'peptide', 14: 'polymyxin',
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15: 'qa_compound', 16: 'quinolone', 17: 'rifampin', 18: 'sulfonamide',
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19: 'tetracenomycin', 20: 'tetracycline', 21: 'trimethoprim', 22: 'tunicamycin'
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}
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short_read_classes = {
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0: 'aminoglycoside', 1: 'bacitracin', 2: 'beta_lactam', 3: 'chloramphenicol',
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4: 'fosfomycin', 5: 'fosmidomycin', 6: 'glycopeptide', 7: 'macrolide-lincosamide-streptogramin',
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8: 'multidrug', 9: 'mupirocin', 10: 'polymyxin', 11: 'quinolone',
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12: 'sulfonamide', 13: 'tetracycline', 14: 'trimethoprim'
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}
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# Streamlit UI
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st.title("Antibiotic Resistance Predictor")
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# st.write("This app predicts antibiotic resistance based on DNA sequences.")
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# Input sequence
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sequence = st.text_area("Enter a DNA sequence:", height=200)
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# Initialize models
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model_long, tokenizer_long = load_model_and_tokenizer("vedantM/NucArg_LongRead")
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model_short, tokenizer_short = load_model_and_tokenizer("vedantM/NucArg_ShortRead")
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if sequence:
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if len(sequence) <= 128:
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chunks = [sequence] # No splitting needed
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model, tokenizer, class_mapping = model_short, tokenizer_short, short_read_classes
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else:
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st.write("Input sequence is too large. Splitting into smaller chunks for processing.")
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chunks = split_sequence(sequence)
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model, tokenizer, class_mapping = model_long, tokenizer_long, long_read_classes
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# Predict for all chunks and aggregate logits
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all_logits = []
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with st.spinner("Predicting..."):
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for chunk in chunks:
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try:
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logits = predict_chunk(model, tokenizer, chunk)
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all_logits.append(logits)
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except Exception as e:
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st.error(f"Error processing chunk: {e}")
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return
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# Aggregate logits
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aggregated_logits = torch.mean(torch.stack(all_logits), dim=0)
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probabilities = torch.softmax(aggregated_logits, dim=-1).tolist()
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predicted_class = torch.argmax(aggregated_logits).item()
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# Display results
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# st.success("Prediction complete!")
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st.write("### Prediction complete!")
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st.success(f"Predicted Class: **{class_mapping[predicted_class]}**")
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st.write("### Class Probabilities")
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type_probabilities = []
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for idx, prob in enumerate(probabilities[0]):
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# Append to the new dataset list
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type_probabilities.append({
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'Type': str(class_mapping[idx]),
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'Probability': float(prob)
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})
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type_probabilities = pd.DataFrame(type_probabilities).sort_values(by='Probability')#,ascending=False)
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# type_probabilities = type_probabilities.set_index('Type')
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tp = type_probabilities.convert_dtypes()
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# st.bar_chart(data=tp, horizontal=True, x='Probability', y='Type')
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# df=px.data.tips()
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fig=px.bar(tp,x='Probability',y='Type', orientation='h')
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st.write(fig)
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if __name__ == "__main__":
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nucArg_app()
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