Version 1
Usage:
MAP.pl -text_data -strategy -window_size -step_size
-fraction_of_proteins
opts:
-text_data This
tab-delimited text file is expected to be a table with 3 columns: (1) Gene symbols,
(2) MS intensities
of sample 1 and (3) MS intensities of sample 2.
-strategy
Trimmed_total_count/Total_count/Pass
-window_size Size
of the sliding window to scan the ratio-intensity plot (similar to the M-A plot
widely used for microarray
data analysis). By default: 400 proteins.
-step_size
Step size of the sliding window. By
default: 100 proteins.
-fraction_of_proteins The fraction of
proteins with the weakest intensity changes of each window used to model technical
variations. They are assumed to be predominantly comprised of non-differentially
expressed
proteins. By default: 50 (values higher than 60 or lower than 30 is not
recommended).
-IN: | Input data |
this tab-delimited text file is expected to be a table with 3 columns: (1) Gene symbols, (2) MS intensities of sample 1 and (3) MS intensities of sample 2. |
-S: | Strategy |
trimmed_total_count/Total_count/Pass |
-W: | Strategy |
size of the sliding window to scan the ratio-intensity plot (similar to the M-A plot widely used for microarray data analysis). By default: 400 proteins. |
-Step: | Step size |
step size of the sliding window. By default: 100 proteins. |
-F: | Fraction_of_proteins |
the fraction of proteins with the weakest intensity changes of each window used to model technical variations. They are assumed to be predominantly comprised of non-differentially expressed proteins. By default: 50 (values higher than 60 or lower than 30 is not recommended). |