Upload 3 files
Browse files- app.py +55 -0
- mutation_model.joblib +3 -0
- requirements.txt +4 -0
app.py
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# app.py
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import gradio as gr
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import joblib
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import numpy as np
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from collections import Counter
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from typing import List
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# helper: k-mer extraction / vectorize (k=3)
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def kmer_counts(seq: str, k=3):
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seq = seq.strip().upper()
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counts = Counter()
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if len(seq) < k:
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return counts
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for i in range(len(seq)-k+1):
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counts[seq[i:i+k]] += 1
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return counts
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def vectorize_single(seq: str, vocab: List[str], k=3):
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x = np.zeros((1, len(vocab)), dtype=float)
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c = kmer_counts(seq, k)
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for j,kmer in enumerate(vocab):
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x[0,j] = c.get(kmer, 0)
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return x
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# load model+vocab (mutation_model.joblib must be uploaded too)
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model, vocab = joblib.load("mutation_model.joblib")
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def predict_sequence(sequence: str):
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if not sequence or len(sequence.strip()) < 3:
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return {"error":"sequence too short"}
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X = vectorize_single(sequence, vocab=vocab, k=3)
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pred = model.predict(X)[0]
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prob = float(model.predict_proba(X).max()) if hasattr(model, "predict_proba") else None
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return {
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"sequence": sequence,
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"mutation_detected": bool(pred),
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"confidence": prob
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}
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# Gradio UI
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with gr.Blocks() as demo:
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gr.Markdown("# DNA Mutation Detector (Quick Space)")
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seq_in = gr.Textbox(label="DNA sequence", placeholder="ATGCGTACGTTAGC...")
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btn = gr.Button("Analyze")
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out = gr.JSON()
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btn.click(fn=predict_sequence, inputs=seq_in, outputs=out)
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# Expose a simple inference API endpoint (Gradio provides /api/predict automatically)
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# but we also expose a programmatic function name for convenience:
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def api_predict(payload: dict):
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seq = payload.get("sequence", "")
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return predict_sequence(seq)
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if __name__ == "__main__":
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demo.launch()
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mutation_model.joblib
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version https://git-lfs.github.com/spec/v1
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oid sha256:cecba933e452e5a139a2f7f7cb85b35976128c42f20e48e26013f3cabfc56d75
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size 305695
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requirements.txt
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gradio>=3.0
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joblib
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numpy
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scikit-learn
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