Spaces:
Sleeping
Sleeping
jennzhuge
commited on
Commit
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a83006f
1
Parent(s):
4e8c8b5
hi
Browse files
app.py
CHANGED
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@@ -11,13 +11,35 @@ def set_default_inputs():
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DEFAULT_INPUTS["latitude"],
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DEFAULT_INPUTS["longitude"])
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with gr.Blocks() as demo:
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# Header section
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gr.Markdown("# DNA Identifier Tool")
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gr.Markdown("
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with gr.Tab("Genus prediction"):
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# Collect inputs for app (DNA and location)
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with gr.Row():
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inp_dna = gr.Textbox(label="DNA", placeholder="e.g. AACAATGTA... (will be automatically truncated to 660 characters)")
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@@ -33,8 +55,13 @@ with gr.Blocks() as demo:
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with gr.Row():
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gr.Markdown('Make plot or table for Top 5 species')
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with gr.Tab('DNA Embedding Space Similarity Visualizer'):
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gr.Markdown("If the highest genus probability is very low for your DNA sequence, we can still examine the DNA embedding of the sequence in relation to known samples or clues.")
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demo.launch()
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DEFAULT_INPUTS["latitude"],
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DEFAULT_INPUTS["longitude"])
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def predict_genus():
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dna_df = pd.read_csv(dna_file.name)
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dnaenv_df = pd.read_csv(dnaenv_file.name)
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results = []
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# envdna_genuses = predict_genus_dna_env(dnaenv_df)
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# dna_genuses = predict_genus_dna(dna_df)
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# images = [get_genus_image(genus) for genus in top_5_genuses]
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genuses = xgboost_infer.infer()
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results.append({
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"sequence": dna_df['nucraw'],
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# "predictions": pd.concat([dna_genuses, envdna_genuses], axis=0)
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'predictions': genuses
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})
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return results
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with gr.Blocks() as demo:
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# Header section
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gr.Markdown("# DNA Identifier Tool")
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gr.Markdown("Welcome to Lofi Amazon Beats' DNA Identifier Tool")
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with gr.Tab("Genus Prediction"):
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gr.Markdown("Input a DNA sequence and the coordinates at which its sample was taken to predict the genus of the DNA. Click 'I'm feeling lucky' to see our predictio for a random sequence.")
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# Collect inputs for app (DNA and location)
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with gr.Row():
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inp_dna = gr.Textbox(label="DNA", placeholder="e.g. AACAATGTA... (will be automatically truncated to 660 characters)")
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with gr.Row():
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gr.Markdown('Make plot or table for Top 5 species')
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with gr.Column():
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genus_out = gr.Dataframe(headers=["DNA", "Coord", "DNA Only Pred Genus", "DNA Only Prob", "DNA & Env Pred Genus", "DNA & Env Prob"])
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btn_run.click(predict_genus, inputs=[inp_dna, inp_lat, inp_lng], outputs=genus_out)
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with gr.Tab('DNA Embedding Space Similarity Visualizer'):
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gr.Markdown("If the highest genus probability is very low for your DNA sequence, we can still examine the DNA embedding of the sequence in relation to known samples or clues.")
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demo.launch()
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