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  sdk: gradio
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- sdk_version: 5.0.0
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  python_version: "3.11"
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@@ -33,8 +33,6 @@ short_description: Explanation-first tri-model genomic variant analysis
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  ## Internal signals extracted
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- From each model β€” nothing redesigned, internal hooks only:
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-
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  - **conv3 activation norm profile** β€” per-nucleotide CNN signal (99 positions)
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  - **Gradient attribution map** β€” input-gradient backward pass
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  - **Mutation-centered peak** β€” activation value at the specific mutation position
@@ -43,17 +41,6 @@ From each model β€” nothing redesigned, internal hooks only:
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  - **Feature ablation response** β€” causal effect of zeroing splice / region / mutation features
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  - **Risk tier classification** β€” PATHOGENIC β†’ BENIGN
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- ## Cross-model explainability metrics
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-
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- | Metric | Description |
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- |---|---|
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- | Mutation Peak Ratio | peak_signal / mean_signal across window |
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- | Counterfactual Magnitude | max probability range across alternatives |
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- | Cross-Model Locality Score | cosine similarity of conv3 profiles |
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- | Signal Concentration Index | fraction of activation within Β±5bp of mutation |
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- | Explainability Strength Score | composite 0–1 score |
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- | Activation Pattern Type | Sharp / Broad / Flat |
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-
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  ## ⚠️ Disclaimer
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  For research use only. Not a clinical diagnostic tool.
 
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  sdk: gradio
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+ sdk_version: 4.44.1
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  python_version: "3.11"
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  app_file: app.py
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  pinned: false
 
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  ## Internal signals extracted
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  - **conv3 activation norm profile** β€” per-nucleotide CNN signal (99 positions)
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  - **Gradient attribution map** β€” input-gradient backward pass
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  - **Mutation-centered peak** β€” activation value at the specific mutation position
 
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  - **Feature ablation response** β€” causal effect of zeroing splice / region / mutation features
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  - **Risk tier classification** β€” PATHOGENIC β†’ BENIGN
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  ## ⚠️ Disclaimer
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  For research use only. Not a clinical diagnostic tool.