procPSMs | R Documentation |
Common routines in PSM processing across search engines.
procPSMs(
dat_dir = NULL,
df = NULL,
scale_rptr_int = FALSE,
rptr_intco = 0,
rptr_intrange = c(0, 100),
rm_craps = FALSE,
rm_krts = FALSE,
rm_allna = FALSE,
annot_kinases = FALSE,
plot_rptr_int = TRUE,
parallel = TRUE
)
dat_dir |
A character string to the working directory. The default is to match the value under the global environment. |
df |
PSM data. |
scale_rptr_int |
Logical; if TRUE, scales (up) MS2 reporter-ion
intensities by MS1 precursor intensity: |
rptr_intco |
Numeric; the threshold of reporter-ion intensity (TMT:
|
rptr_intrange |
Numeric vector at length two. The argument specifies the
range of reporter-ion intensities (TMT: |
rm_craps |
Logical; if TRUE, cRAP proteins will be removed. The default is FALSE. |
rm_krts |
Logical; if TRUE, keratin entries will be removed. The default is FALSE. |
rm_allna |
Logical; if TRUE, removes data rows that are exclusively NA
across ratio columns of |
annot_kinases |
Logical; if TRUE, proteins of human or mouse origins will be annotated with their kinase attributes. The default is FALSE. |
plot_rptr_int |
Logical; if TRUE, the distributions of reporter-ion intensities will be plotted. The default is TRUE. The argument is also applicable to the precursor intensity with MaxQuant LFQ. |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.