Description Usage Arguments Value Examples
View source: R/SpectronauttoMSstatsLiPFormat.R
Takes as as input both raw LiP and Trp outputs from Spectronautt.
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 | SpectronauttoMSstatsLiPFormat(
LiP.data,
fasta,
Trp.data = NULL,
annotation = NULL,
intensity = "PeakArea",
filter_with_Qvalue = TRUE,
qvalue_cutoff = 0.01,
useUniquePeptide = TRUE,
removeFewMeasurements = TRUE,
removeProtein_with1Feature = FALSE,
removeNonUniqueProteins = TRUE,
removeModifications = TRUE,
removeiRT = TRUE,
summaryforMultipleRows = max,
which.Conditions = "all",
use_log_file = FALSE,
append = FALSE,
verbose = TRUE,
log_file_path = NULL,
base = "MSstatsLiP_log_"
)
|
LiP.data |
name of LiP Spectronaut output, which is long-format. |
fasta |
A string of path to a FASTA file, used to match LiP peptides. |
Trp.data |
name of TrP Spectronaut output, which is long-format. |
annotation |
name of 'annotation.txt' data which includes Condition, BioReplicate, Run. If annotation is already complete in Spectronaut, use annotation=NULL (default). It will use the annotation information from input. |
intensity |
'PeakArea'(default) uses not normalized peak area. 'NormalizedPeakArea' uses peak area normalized by Spectronaut |
filter_with_Qvalue |
TRUE(default) will filter out the intensities that have greater than qvalue_cutoff in EG.Qvalue column. Those intensities will be replaced with zero and will be considered as censored missing values for imputation purpose. |
qvalue_cutoff |
Cutoff for EG.Qvalue. default is 0.01. |
useUniquePeptide |
TRUE(default) removes peptides that are assigned for more than one proteins. We assume to use unique peptide for each protein. |
removeFewMeasurements |
TRUE (default) will remove the features that have 1 or 2 measurements across runs. |
removeProtein_with1Feature |
TRUE will remove the proteins which have only 1 feature, which is the combination of peptide, precursor charge, fragment and charge. FALSE is default. |
removeNonUniqueProteins |
TRUE will remove proteins that were not uniquely identified. IE if the protein column contains multiple proteins seperated by ";". TRUE is default |
removeModifications |
TRUE will remove peptide that contain a modification. Modification must be indicated by "[". TRUE is default |
removeiRT |
TRUE will remove proteins that contain iRT. True is default |
summaryforMultipleRows |
max(default) or sum - when there are multiple measurements for certain feature and certain run, use highest or sum of multiple intensities. |
which.Conditions |
list of conditions to format into MSstatsLiP format. If "all" all conditions will be used. Default is "all". |
use_log_file |
logical. If TRUE, information about data processing will be saved to a file. |
append |
logical. If TRUE, information about data processing will be added to an existing log file. |
verbose |
logical. If TRUE, information about data processing will be printed to the console. |
log_file_path |
character. Path to a file to which information about
data processing will be saved.
If not provided, such a file will be created automatically.
If |
base |
start of the file name. |
a list
of two data.frames
in MSstatsLiP format
1 2 3 4 5 6 7 8 9 10 11 | # Output datasets of Spectronaut
head(LiPRawData)
head(TrPRawData)
fasta_path <- system.file("extdata", "ExampleFastaFile.fasta", package="MSstatsLiP")
MSstatsLiP_data <- SpectronauttoMSstatsLiPFormat(LiPRawData,
fasta_path,
TrPRawData)
head(MSstatsLiP_data[["LiP"]])
head(MSstatsLiP_data[["TrP"]])
|
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