rewirebio.iobenchmarks
Protocol

OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)

Accuracy, sensitivity, specificity, PPV and NPV of 17 predictors using default categorical calls.

17 evaluations · 85 results

Overview

Accuracy, sensitivity, specificity, PPV and NPV of 17 predictors using default categorical calls.

Consult the linked sources for architecture or protocol details. Missing evidence is not evidence of a missing capability.

17 recorded evaluations, 85 metric rows. A comparison chart has not yet been validated for these results. The table retains the individual findings and their sources.

View coverage and remaining gaps across all benchmarks

Results

Results are available, but no reviewed comparison panel is linked in this release.

All evaluations

17 evaluations · 85 results. Different protocols are not a single leaderboard.

Filter evaluations

Applied filters: All linked evaluations

Exact evaluated configurations and original reported results
Tested configurationProtocol and datasetFindingEvidence and details
Configuration: CanDrA (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.49 accuracy
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

CanDrA on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), B18; Algorithm 'CanDrA'; column 'Accuracy (±2σ)'
Configuration: CanDrA (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.46 negative-predictive-value
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

CanDrA on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), F18; Algorithm 'CanDrA'; column 'NPV (±2σ)'
Configuration: CanDrA (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.49 precision
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

CanDrA on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), E18; Algorithm 'CanDrA'; column 'PPV (±2σ)'
Configuration: CanDrA (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.8 recall
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

CanDrA on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), C18; Algorithm 'CanDrA'; column 'Sensitivity (±2σ)'
Configuration: CanDrA (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.17 specificity
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Author-reported evaluation · Source checked
Methods, coverage and source

CanDrA on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), D18; Algorithm 'CanDrA'; column 'Specificity (±2σ)'
Configuration: DEOGEN2 (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.7 accuracy
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

DEOGEN2 on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), B2; Algorithm 'DEOGEN2'; column 'Accuracy (±2σ)'
Configuration: DEOGEN2 (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.79 negative-predictive-value
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

DEOGEN2 on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), F2; Algorithm 'DEOGEN2'; column 'NPV (±2σ)'
Configuration: DEOGEN2 (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.65 precision
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

DEOGEN2 on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), E2; Algorithm 'DEOGEN2'; column 'PPV (±2σ)'
Configuration: DEOGEN2 (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.87 recall
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

DEOGEN2 on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), C2; Algorithm 'DEOGEN2'; column 'Sensitivity (±2σ)'
Configuration: DEOGEN2 (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.51 specificity
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

DEOGEN2 on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), D2; Algorithm 'DEOGEN2'; column 'Specificity (±2σ)'
Configuration: FATHMM-disease (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.52 accuracy
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-disease on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), B17; Algorithm 'FATHMM-disease'; column 'Accuracy (±2σ)'
Configuration: FATHMM-disease (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.53 negative-predictive-value
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-disease on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), F17; Algorithm 'FATHMM-disease'; column 'NPV (±2σ)'
Configuration: FATHMM-disease (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.51 precision
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-disease on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), E17; Algorithm 'FATHMM-disease'; column 'PPV (±2σ)'
Configuration: FATHMM-disease (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.63 recall
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-disease on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), C17; Algorithm 'FATHMM-disease'; column 'Sensitivity (±2σ)'
Configuration: FATHMM-disease (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.42 specificity
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-disease on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), D17; Algorithm 'FATHMM-disease'; column 'Specificity (±2σ)'
Configuration: FATHMM-MKL (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.6 accuracy
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-MKL on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), B11; Algorithm 'FATHMM-MKL'; column 'Accuracy (±2σ)'
Configuration: FATHMM-MKL (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.93 negative-predictive-value
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-MKL on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), F11; Algorithm 'FATHMM-MKL'; column 'NPV (±2σ)'
Configuration: FATHMM-MKL (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.56 precision
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-MKL on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), E11; Algorithm 'FATHMM-MKL'; column 'PPV (±2σ)'
Configuration: FATHMM-MKL (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.98 recall
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-MKL on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), C11; Algorithm 'FATHMM-MKL'; column 'Sensitivity (±2σ)'
Configuration: FATHMM-MKL (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.21 specificity
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-MKL on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), D11; Algorithm 'FATHMM-MKL'; column 'Specificity (±2σ)'
Configuration: FATHMM-XF (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.66 accuracy
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-XF on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), B4; Algorithm 'FATHMM-XF'; column 'Accuracy (±2σ)'
Configuration: FATHMM-XF (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.85 negative-predictive-value
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-XF on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), F4; Algorithm 'FATHMM-XF'; column 'NPV (±2σ)'
Configuration: FATHMM-XF (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.6 precision
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-XF on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), E4; Algorithm 'FATHMM-XF'; column 'PPV (±2σ)'
Configuration: FATHMM-XF (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.93 recall
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-XF on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), C4; Algorithm 'FATHMM-XF'; column 'Sensitivity (±2σ)'
Configuration: FATHMM-XF (Chen et al. 2020)Protocol: OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020 Additional file 10)
Dataset: OncoKB-annotated somatic missense mutations (oncogenic, likely oncogenic and likely neutral)
0.39 specificity
fraction · higher

Uncertainty: Not yet extracted: Printed as 'mean (lower-upper)' under the column header '(±2σ)': per Methods, the mean and two standard deviations over 100 random draws. That is not a confidence interval, and the schema's standard_deviation type would need a standard deviation derived from rounded bounds, so no structured uncertainty is recorded. The printed range is kept in printed_source_cell; every range is symmetric about the mean to rounding.

Coverage: Not reported scored / Not reported eligible

Independent external evaluation · Source checked
Methods, coverage and source

FATHMM-XF on OncoKB benchmark (positive set not stated), default categorical calls (Chen et al. 2020)

somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

Aggregation: Not reported

Comprehensive assessment of computational algorithms in predicting cancer driver mutations; Chen et al. 2020, Additional file 10: Performance metrics of 17 algorithms, default categories, benchmark 2 (OncoKB) · Additional file 10 (sheet 'Additional_file_10'), D4; Algorithm 'FATHMM-XF'; column 'Specificity (±2σ)'

Source checking is not independent reproduction. Release 2026-10-10-7fcc3e48a123.

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Stable ID: somatic-oncogenicity-20261009-protocol-chen2020-oncokb-default

areas
dna-genomes
contexts
clinical_research
protocol
Binary predictions by default categorical calls (categories in Additional file 1) compared with the truth labels with reportROC; 400 positives and 400 negatives sampled 100 times; mean and two standard deviations reported.
version
Additional file 10
metric
accuracy
limitations
Binary metrics are means over 100 random draws of 400 positives and 400 negatives; the bracketed range is the mean plus or minus two standard deviations, not a confidence interval.; Predictor scores date from dbNSFP v4.0 and 2019 web servers; current releases (for example AlphaMissense, CHASMplus, BoostDM) are not included.; Only 17 algorithms provide default categories, mostly germline deleteriousness tools; cancer-specific tools other than CanDrA and FATHMM-disease are absent.; OncoKB annotations are biased towards known, often actionable cancer genes (Discussion).; Some predictors were trained on known cancer mutations, so performance on literature-curated drivers may be inflated.; The OncoKB set has 421 or 497 likely neutral negatives (Methods and Results disagree) and 400 are drawn per repeat, so the draws overlap heavily and the spread understates sampling uncertainty. Results and Methods also disagree on the positive counts, and which positive set fed the binary metrics is not stated.; Two authors (H. Liang, G.B. Mills) co-developed CanDrA (reference 7), and the cell viability labels come from the same group's assays; CanDrA rows are author_reported.
source locator
Additional file 10; Methods 'Calculation of five evaluation metrics based on categorical predictions'
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