## ToxoLopit data
library("MSnbase")
library("pRoloc")
csvfile <- "../../inst/extdata/TL123_complete.csv"
pDatacsv <- "../../inst/extdata/ToxoLOPIT_pData.csv"
csv <- read.csv(csvfile, sep = "")
csvpdata <- read.csv(pDatacsv)
Barylyuk2020ToxoLopit <- readMSnSet2(csvfile, ecol = 2:31, sep ="\t", fnames = 1)
## Experimental data to add
experiment <- new("MIAPE",
lab = "Department of Biochemistry, University of Cambridge, Cambridge, UK; Cambridge Centre for Proteomics, University of Cambridge, Cambridge, UK",
name = "Konstantin Barylyuk",
contact = "Konstantin Barylyuk, Ross F. Waller",
email = "kb601@cam.ac.uk, rfw26@cam.ac.uk",
samples = list(
species = "Toxoplasma gondii, strain RH",
operator = "Konstantin Barylyuk"
),
title = "Whole-cell spatial proteome of Toxoplasma: molecular anatomy of an apicomplexan cell",
abstract = "",
pubMedIds = "",
url = "",
instrumentModel = "Orbitrap Fusion Lumos",
instrumentManufacturer = "ThermoScientific",
ionSource = "",
analyser = "Orbitrap",
detectorType = "Orbitrap",
softwareName = "Mascot, Proteome Discoverer",
collisionEnergy = "",
dateStamp = "16 March 2020"
)
## Expression data
e <- exprs(Barylyuk2020ToxoLopit)
## Experiment info
toName <- paste0(colnames(e)[1:30])
colnames(e) <- toName
pd <- data.frame(toName,
row.names=colnames(e), csvpdata)
pd <- new("AnnotatedDataFrame", pd)
process <- new("MSnProcess",
processing=c(
paste("Loaded on ",date(),".",sep=""),
paste("VSN Normalisation")),
normalised=TRUE)
Barylyuk2020ToxoLopit <- new("MSnSet",
exprs = e,
phenoData = pd,
experimentData = experiment,
featureData = new("AnnotatedDataFrame", fData(Barylyuk2020ToxoLopit)))
plot2D(Barylyuk2020ToxoLopit)
Barylyuk2020ToxoLopit@processingData <- process
stopifnot(validObject(Barylyuk2020ToxoLopit))
save(Barylyuk2020ToxoLopit, file="../../data/Barylyuk2020ToxoLopit.rda",
compress = "xz", compression_level = 9)
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