View source: R/stats_summary.R
summarise_stats | R Documentation |
In most cases, you probably want to use the export_stats_genesummary()
function instead.
That is a wrapper function that uses this function but also adds additional functionality.
For documentation on the output table, also refer to that function.
summarise_stats(
dataset,
return_dea = TRUE,
return_diffdetect = FALSE,
dea_logfc_as_effectsize = FALSE,
diffdetect_zscore_threshold = 6,
diffdetect_type = "auto"
)
dataset |
dataset where dea() and/or differential_detect() has been applied |
return_dea |
boolean, set to TRUE to include DEA results in the stats table that returns 1 value per gene (setting TRUE for both DEA and DD will merge results) |
return_diffdetect |
analogous to |
dea_logfc_as_effectsize |
optionally, the resulting effectsize column can be populated with standardized foldchange values (effectsize = log2fc / sd(log2fc)). When including differential detection results this'll be a convenient approach to getting 1 standardized distribution of DEA+DD effectsizes that can be used in e.g. GO analyses. While this is unusual, one could e.g. use this for DEA algorithms that apply shrinkage to estimated foldchanges such as MSqRob |
diffdetect_zscore_threshold |
differential detect z-score cutoff. A typical value would be 5 or 6 (default) To plot histograms of the respective z-score distributions and inspect potential cutoff values for this relatively arbitrary metric, see below example code |
diffdetect_type |
type of differential detect scores. options: 'auto' = set to 'detect' if this score is available, 'quant' otherwise 'detect' = differential detection z-scores computed from only "detected" peptides (no MBR) 'quant' = differential detection z-scores computed from all quantified peptides (uses MBR) |
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