68 research outputs found

    Feature optimization for GBM. Plotted are the areas under the curves (AUCs) of the receiver operator characteristics acquired through our incremental feature selection process.

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    <p>Three sets of AUCs are computed from the 10-fold cross-validation (CV) of the training set GBM.Ex (dotted line) and the independent validation (IV) of 2 test sets, GBM.S1 and GBM.S2 (solid and dashed line). On the x-axis are features that are incrementally selected. The dashed box marks the peaks of the cross-validation AUC, which corresponds to the optimal feature set used for CanDrA.</p

    Feature optimization for OVC. Plotted are the areas under the curves (AUCs) of the receiver operator characteristics acquired through our incremental feature selection process.

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    <p>Three sets of AUCs are computed from the 10-fold cross-validation (CV) of the training set OVC.Ex (dotted line) and the independent validation (IV) of 2 test sets, OVC.S1 and OVC.S2 (solid and dashed line). On the x-axis are features that are incrementally selected. The dashed box marks the peaks of the cross-validation AUC, which corresponds to the optimal feature set used for CanDrA.</p

    Correlation between mutation score and prevalence.

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    <p>Twelve algorithms (x-axis) were compared using 4 data sets: (a) GBM mutations in <i>TP53</i>, (b) GBM mutations in <i>PTEN</i>, (c) OVC mutations in <i>TP53</i>, and (d) OVC mutations in <i>KRAS</i>.</p

    Additional file 6: Figure S2. of Hotspot mutations delineating diverse mutational signatures and biological utilities across cancer types

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    The significance of overlap (y-axis, calculated using Fisher exact test) between hotspot-mutation-containing-genes and previously known cancer genes at various adjusted p value cutoffs (x-axis). (PDF 37 kb
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