Prepare the data for making MA plots
Usage
prepare_MA_data(
res,
label = NULL,
ns_color = "grey70",
up_color = "red3",
down_color = "dodgerblue"
)
Arguments
- res
A data frame with results from get_DEPresults()
- label
Specifies which points to label. The default is 'sig', labeling all significant points. Entering a value for top_n limits the labeling to the top_n up- and top_n down-regulated proteins based on the p.adj. When providing a vector with protein names, only those points are labeled.
- ns_color
Specifies the color of non-significant proteins.
- up_color
Specifies the color of the significantly up-regulated proteins.
- down_color
Specifies the color of the significantly down-regulated proteins.
Examples
se <- prepare_se(report.pg_matrix, expDesign)
#> Imputing along margin 1 (features/rows).
#> Warning: 36 rows with more than 50 % entries missing;
#> mean imputation used for these rows
#> Cluster size 5548 broken into 2203 3345
#> Cluster size 2203 broken into 1569 634
#> Cluster size 1569 broken into 1504 65
#> Cluster size 1504 broken into 645 859
#> Done cluster 645
#> Done cluster 859
#> Done cluster 1504
#> Done cluster 65
#> Done cluster 1569
#> Done cluster 634
#> Done cluster 2203
#> Cluster size 3345 broken into 2136 1209
#> Cluster size 2136 broken into 1087 1049
#> Done cluster 1087
#> Done cluster 1049
#> Done cluster 2136
#> Done cluster 1209
#> Done cluster 3345
se <- add_median_peptide_intensity(se, report.pr_matrix)
res <- get_DEPresults(se, type = 'all')
#> Tested contrasts: neg_ctrl_vs_motif1, neg_ctrl_vs_motif2, motif1_vs_motif2
data <- prepare_MA_data(res)