estimateMasterFdr | R Documentation |
This function takes all possible combination of pepfiles
of length greater or equal than 2 and computes the number of
estimated incorrect peptides, the number of unique peptides,
the number of unique protetypic peptides and the
false discovery rate after merging for each combination.
The best combination has an fdr lower than masterFdr
and the highest number of unique (proteotypic) peptides.
estimateMasterFdr(pepfiles, fastafile, masterFdr = 0.025, fdr = 0.01, proteotypic = TRUE, missedCleavages = 0, IisL = FALSE, maxFileComb = length(pepfiles), verbose = interactive())
pepfiles |
A |
fastafile |
A |
masterFdr |
A |
fdr |
Peptide FDR level for individual peptide files filtering. |
proteotypic |
Logical. Should number proteotypic peptides be used to choose best combination and plot results or total number of unique peptides. |
missedCleavages |
Number of maximal missed cleavage sites. Default is 0. |
IisL |
If |
maxFileComb |
A |
verbose |
Should progress messages be printed? |
The false discovery rate for the master (merged) file is calcualted
by summing the number of estimated false discoveries for each
individual final peptide file (number of unique peptides in that file
multiplied by fdr
) divided by the total number of unique
peptides for that specific combination.
The function returns an instance of the class
"MasterFdrResults"
.
An instance of class "MasterFdrResults"
.
See details above.
Laurent Gatto
Bond N. J., Shliaha P.V., Lilley K.S. and Gatto L., (2013) J. Prot. Research.
The makeMaster
function to combine
the peptide data as suggested by estimateMasterFdr
into
one single master peptide file.
The vignette, accessible with synapterGuide()
illustrates a
complete pipeline using estimateMasterFdr
and
makeMaster
.
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