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Update index.html

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@@ -1570,26 +1570,30 @@ kbd {
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  <div class="card-header">
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  <div class="card-header-icon"><i class="fas fa-check-circle"></i></div>
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  <div class="card-header-title">Classifier Performance Metrics</div>
 
 
 
 
 
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  </div>
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  <div class="card-body">
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- <p class="prose">Metrics obtained on a held-out test set, never seen during model training or hyperparameter tuning.</p>
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  <table class="metrics-table">
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  <thead><tr><th>Metric</th><th>Value</th><th>Description</th></tr></thead>
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  <tbody>
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- <tr><td>Accuracy</td><td><span class="metric-val">0.963</span></td><td>Proportion of correctly classified sequences (AMP &amp; Non-AMP).</td></tr>
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- <tr><td>Precision</td><td><span class="metric-val">0.964</span></td><td>Of all predicted AMPs, the fraction that are truly AMPs (fewer false positives).</td></tr>
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- <tr><td>Recall</td><td><span class="metric-val">0.963</span></td><td>Of all true AMPs, the fraction correctly identified (fewer false negatives).</td></tr>
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- <tr><td>F1-Score</td><td><span class="metric-val">0.963</span></td><td>Harmonic mean of precision and recall — balanced performance indicator.</td></tr>
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- <tr><td>Validation Accuracy</td><td><span class="metric-val">0.968</span></td><td>Accuracy on the validation split used during model development.</td></tr>
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  </tbody>
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  </table>
 
 
 
 
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  </div>
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  </div>
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- <div class="card">
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- <div class="card-header">
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- <div class="card-header-icon"><i class="fas fa-vials"></i></div>
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- <div class="card-header-title">MIC Regressor Metrics (per bacterium)</div>
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- </div>
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  <div class="card-body">
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  <p class="prose">Separate regression models predict MIC for each organism. Performance evaluated via MSE (log-scale), R², Pearson correlation, and Kendall's tau.</p>
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  <table class="metrics-table">
@@ -1663,7 +1667,7 @@ kbd {
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  <div class="card-body">
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  <p class="prose">This web application provides a streamlined interface for classifying amino acid sequences as Antimicrobial Peptides (AMPs) or Non-AMPs, and for predicting the Minimum Inhibitory Concentration (MIC) of potential AMPs against clinically relevant bacteria. AMPs are key components of the innate immune system and represent a promising avenue for combating drug-resistant pathogens.</p>
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  <div class="section-h3">Model Selection Criteria</div>
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- <p class="prose">Over 225 combinations of feature extraction and selection methods were evaluated across four machine learning architectures for each target organism. The final models were selected based on:</p>
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  <ul class="prose" style="margin-left:18px;">
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  <li><strong>High Accuracy, F1-score, and Validation Accuracy</strong> on a held-out test set.</li>
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  <li><strong>Robustness to sequence length variation</strong> within the 10–100 aa range.</li>
 
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  <div class="card-header">
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  <div class="card-header-icon"><i class="fas fa-check-circle"></i></div>
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  <div class="card-header-title">Classifier Performance Metrics</div>
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+ <<div class="card">
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+ <div class="card-header">
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+ <div class="card-header-icon"><i class="fas fa-check-circle"></i></div>
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+ <div class="card-header-title">MLP Classifier Performance Metrics</div>
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+ <div class="card-header-sub">Architecture: Multi-Layer Perceptron (MLP)</div>
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  </div>
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  <div class="card-body">
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+ <p class="prose">Best-trial results from MLP hyperparameter search (trial #49) on AAC + CTD features with RFE selection. Metrics reflect training and validation performance of the final selected model.</p>
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  <table class="metrics-table">
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  <thead><tr><th>Metric</th><th>Value</th><th>Description</th></tr></thead>
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  <tbody>
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+ <tr><td>Training Accuracy</td><td><span class="metric-val">0.9941</span></td><td>Proportion of correctly classified sequences on the training set.</td></tr>
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+ <tr><td>Validation Accuracy</td><td><span class="metric-val">0.9682</span></td><td>Accuracy on the held-out validation split used during model development.</td></tr>
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+ <tr><td>Training Loss</td><td><span class="metric-val">0.0412</span></td><td>Binary cross-entropy loss on the training set (lower is better).</td></tr>
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+ <tr><td>Validation Loss</td><td><span class="metric-val">0.1261</span></td><td>Binary cross-entropy loss on the validation set.</td></tr>
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+ <tr><td>Loss Gap</td><td><span class="metric-val">0.0849</span></td><td>Difference between validation and training loss small gap indicates limited overfitting.</td></tr>
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  </tbody>
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  </table>
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+ <p class="prose" style="margin-top:14px;font-size:12px;color:var(--text-muted);">
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+ <i class="fas fa-info-circle"></i>
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+ <strong>Architecture:</strong> 1 hidden layer · 256 units · ReLU activation · L2 regularisation (1e-5) · Dropout 0.3 · Learning rate 1e-3
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+ </p>
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  </div>
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  </div>
 
 
 
 
 
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  <div class="card-body">
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  <p class="prose">Separate regression models predict MIC for each organism. Performance evaluated via MSE (log-scale), R², Pearson correlation, and Kendall's tau.</p>
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  <table class="metrics-table">
 
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  <div class="card-body">
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  <p class="prose">This web application provides a streamlined interface for classifying amino acid sequences as Antimicrobial Peptides (AMPs) or Non-AMPs, and for predicting the Minimum Inhibitory Concentration (MIC) of potential AMPs against clinically relevant bacteria. AMPs are key components of the innate immune system and represent a promising avenue for combating drug-resistant pathogens.</p>
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  <div class="section-h3">Model Selection Criteria</div>
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+ <p class="prose">Over 225 combinations of feature extraction and selection methods were evaluated across four machine learning architectures for each target organism. The final classifier is a <strong>Multi-Layer Perceptron (MLP)</strong> trained on AAC + CTD features with RFE-based feature selection. The final models were selected based on:</p>
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  <ul class="prose" style="margin-left:18px;">
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  <li><strong>High Accuracy, F1-score, and Validation Accuracy</strong> on a held-out test set.</li>
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  <li><strong>Robustness to sequence length variation</strong> within the 10–100 aa range.</li>