Compute extended ranking across 11 classification + OpDEA metrics
Source:R/Benchmarking_Multiple.R
bm_compute_extended_ranking.RdFor each of the 11 metrics, averages across comparisons per Assay (mean), then ranks methods in descending order (higher = better for all metrics). Final rank = mean of the 11 individual ranks.
Usage
bm_compute_extended_ranking(
opdea_combined,
bench_metrics_combined,
metrics = .BM_EXTENDED_METRICS
)Value
Named list with:
- extended_combined
Merged data.frame (long format)
- mean_aggregated
data.frame of mean metric values per Assay
- mean_ranking
data.frame with rank columns and rank_final
- n_methods
Number of unique methods
- n_comparisons
Number of unique comparisons
- metrics_used
Metrics actually used
Details
Note: this extended ranking can drift away from the canonical OpDEA ranking
(bm_compute_ranking, based on nMCC/G_mean/pAUC). Performance is collinear
with F1 (so F1 effectively counts twice), and in spike-in designs
Accuracy/NPV are dominated by the background (TN >> ), hence they have
little discriminative power. Use it as a complementary view, not as a
substitute for the OpDEA ranking.
Examples
data(nadia_dia)
sp <- utils::read.delim(system.file("extdata", "nadia_dia_spikein.tsv.gz",
package = "NADIA"))
ev <- data.frame(Comparison = rep(c("B-A", "D-A"), each = 2),
Species = c("ECOLI", "YEAST"),
expected_logFC = c(1, -0.58, 2, -3.3))
opdea_all <- NULL
bench_all <- NULL
for (nm in c("cycloess", "quantile")) {
de <- process_proteomics(nadia_dia, norm_method = nm,
verbose = FALSE)$DEPs_results
de$Species <- sp$PG.OrganismId[match(de$Protein.IDs, sp$PG.ProteinGroups)]
opdea_all <- rbind(opdea_all, cbind(compute_opdea_metrics(de, ev), Assay = nm))
bench_all <- rbind(bench_all, cbind(compute_benchmark_metrics(de, ev), Assay = nm))
}
ext <- bm_compute_extended_ranking(opdea_all, bench_all)
ext$mean_ranking[, c("Assay", "rank_final")]
#> Assay rank_final
#> 1 cycloess 1.09
#> 2 quantile 1.91