Precision medicine exploits genetic differences to tailor drug treatments. Here the authors mapped ~1.17 M variants near drug-binding sites, built SNPdrug3D, and showed such variants often disrupt ...
data = st.io.read_gef(file_path="../processed_data/B01809C2/GeneExpMatrix/B01809C2.cellbin.gef", # maximum number of counts required for a cell to pass fitlering. max ...
The toolkit reads tidy CSV annotation files and produces agreement metrics, label-distribution analysis, disagreement tables, plots, and a Markdown report. It is designed for human-evaluation ...
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