run.diann | R Documentation |
Runs a DIA-NN analysis of the selected DIA-file and input library in TSV format
run.diann( diannPath, diaFile, libFile, output = NULL, matrices = T, matQ = 0.01, threads = detectCores(), fasta = NULL, enzyme, separateMassAcc = F, massAcc = NULL, reportLibInfo = T, robustLC = NULL, relaxProtInf = F, carbamidomethyl_C = T, nativeLib = F, matchBetweenRuns = F )
diannPath |
Absolute path to the DIA-NN executable |
diaFile |
Absolute path to the input DIA raw file |
libFile |
Absolute path to the input spectral library file (as given by the make.osw.lib function) |
output |
Desired file name for DIA-NN reports (incl. absolute path) |
matrices |
A logical determining if quantitative matrices for proteins and precursors should be outputted (Default=TRUE). |
matQ |
numeric in the range c(0,1) setting the q-value to use for filtering matrices. |
threads |
Integer specifying the number of threads for the analysis |
fasta |
Absolute path to a FASTA file for matching of peptides sequences to proteins |
enzyme |
Character specifying the enzyme to use for in-silico digestion of sequences in the FASTA file |
separateMassAcc |
should mass accuracy be determined for each individual MS file (logical) |
massAcc |
Numeric setting the desired MS1 accuracy |
reportLibInfo |
Logical determining if extra info on fragment ions and precursors should be saved to main report (default TRUE) |
robustLC |
Specfies whether Quantification should be run in Robust LC mode. Possible values are "high_accuracy" or "high_precision". Default = NULL. |
relaxProtInf |
Logical determining if relaxed protein inference should be enabled. Default = FALSE |
carbamidomethyl_C |
Carbamidomethyl on Cysteine residues as fixed modification. Default = T. |
nativeLib |
Logical setting if the spectral library is a native library or not. |
matchBetweenRuns |
logical determining if match-between-runs (MBR) should be enabled. (Default = FALSE) |
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