Compare peptide abundances between conditions
compare.RdPerforms differential abundance analysis on proteomics data. Supports three methods: GLM (default), ART (non-parametric), and pairwise tests.
Arguments
- data
A pepdiff_data object from [read_pepdiff()]
- ...
Additional arguments passed to methods
- compare
Factor to compare (character string)
- ref
Reference level for comparisons
- within
Optional factor(s) to stratify by
- method
Analysis method: "glm" (default), "art", or "pairwise"
- test
For pairwise method: "wilcoxon", "bootstrap_t", "bayes_t", or "rankprod"
- alpha
Significance threshold (default 0.05). Used for p-value based tests.
- fdr_method
FDR correction method (default "BH"). Not applied for bayes_t.
- bf_threshold
Bayes factor threshold for significance (default 3). Only used when test = "bayes_t". BF > threshold marks peptide as significant.
Value
A pepdiff_results object containing:
- results
Tibble with peptide, gene_id, comparison, fold_change, log2_fc, p_value, fdr, significant. For bayes_t: p_value/fdr are NA, includes bf and evidence columns.
- comparisons
Tibble defining the comparisons made
- method
Statistical method used
- diagnostics
Model convergence information (for GLM/ART)
- params
Analysis parameters
- data
The original pepdiff_data object
- call
The function call
Examples
if (FALSE) { # \dontrun{
# Simple comparison
results <- compare(data, compare = "treatment", ref = "ctrl")
# Stratified comparison
results <- compare(data, compare = "treatment", ref = "ctrl", within = "timepoint")
# Pairwise test
results <- compare(data, compare = "treatment", ref = "ctrl",
method = "pairwise", test = "wilcoxon")
# Bayes factor test (uses bf_threshold instead of alpha/FDR)
results <- compare(data, compare = "treatment", ref = "ctrl",
method = "pairwise", test = "bayes_t", bf_threshold = 10)
} # }