Create omni_genomics.py
Browse files- omni_genomics.py +70 -0
omni_genomics.py
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import plotly.express as px
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import plotly.graph_objects as go
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import pandas as pd
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import numpy as np
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class OMNIGenomics:
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def __init__(self):
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pass
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def plot_variant_density(self, vcf_df):
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"""
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Creates a high-fidelity visualization of variant distribution
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across the chromosomal landscape.
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"""
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if vcf_df.empty:
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return go.Figure()
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# Sort by Chromosome and Position
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vcf_df = vcf_df.sort_values(["Chromosome", "Position"])
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# Create the Density Map
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fig = px.density_heatmap(
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vcf_df,
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x="Position",
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y="Chromosome",
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z="Risk_Score",
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histfunc="avg",
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color_continuous_scale="Viridis",
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title="Chromosomal Variant Density & Risk Distribution",
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labels={'Risk_Score': 'Impact Level'},
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nbinsx=100,
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nbinsy=22
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)
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# Apply Stealth/V9 Styling
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fig.update_layout(
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paper_bgcolor='rgba(0,0,0,0)',
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plot_bgcolor='rgba(0,0,0,0)',
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font_color="#e0e0e0",
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xaxis=dict(showgrid=False, zeroline=False),
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yaxis=dict(showgrid=False, zeroline=False, autorange="reversed"),
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coloraxis_colorbar=dict(title="Risk Score")
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)
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return fig
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def plot_pharmacogenomic_markers(self, markers):
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"""
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Visualizes specific drug-gene interaction alerts.
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"""
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# Simulated data if none provided
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if not markers:
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markers = {'CYP2C19': 0.9, 'VKORC1': 0.7, 'SLCO1B1': 0.4}
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fig = px.bar(
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x=list(markers.keys()),
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y=list(markers.values()),
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color=list(markers.values()),
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color_continuous_scale="Reds",
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title="Pharmacogenomic Toxicity/Efficacy Markers",
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labels={'x': 'Gene', 'y': 'Alert Intensity'}
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)
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fig.update_layout(
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paper_bgcolor='rgba(0,0,0,0)',
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plot_bgcolor='rgba(0,0,0,0)',
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font_color="#e0e0e0"
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)
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return fig
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