####---- Zhu et al. 2018, Nature Communications - HeLa dilutions ----####
## Zhu, Ying, Paul D. Piehowski, Rui Zhao, Jing Chen, Yufeng Shen, Ronald J.
## Moore, Anil K. Shukla, et al. 2018. “Nanodroplet Processing Platform for Deep
## and Quantitative Proteome Profiling of 10-100 Mammalian Cells.” Nature
## Communications 9 (1): 882.
library(SingleCellExperiment)
library(scp)
library(tidyverse)
dataDir <- "~/PhD/.localdata/SCP/zhu2018NC_hela/"
## The data was downloaded from ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2018/01/PXD006847
## to scpdata/inst/extdata/zhu2018NC_hela
####---- Get the annotation data ----####
## The annotation file was manually created from the samples names and
## the available information from the methods section
annot <- read.csv(paste0(dataDir, "sample_annotation.csv"),
row.names = "SampleName")
####---- Peptide data ----####
## Load the quantification data
peps <- read.table(paste0(dataDir, "CulturedCells_peptides.txt"),
sep = "\t", header = TRUE)
peps <- readSingleCellExperiment(peps,
ecol = grep("^Intensity.", colnames(peps)),
fnames = "Sequence")
colnames(peps) <- gsub("Intensity.", "", colnames(peps))
####---- Protein data ----####
## Load the quantification data
prots <- read.table(paste0(dataDir, "CulturedCells_proteinGroups.txt"),
sep = "\t", header = TRUE)
## Remove unnecessary columns
sel <- !grepl("Peptides.*[HMT]|^Identif|^Razor.*[HMT]|Sequence.*[HMT]|Unique.*[HMT]|MS.MS.*[HMT]",
colnames(prots))
prots <- prots[, sel]
## Split protein data based on the quantification method:
## 1. Protein intensity
protsInt <- prots[, !grepl("^iBAQ|^LFQ", colnames(prots))]
protsInt <- readSingleCellExperiment(protsInt,
ecol = grep("^Intensity.", colnames(protsInt)),
fnames = "Protein.IDs")
colnames(protsInt) <- gsub("Intensity.", "", colnames(protsInt))
## 2. LFQ
protsLFQ <- prots[, !grepl("^iBAQ|^Intensity", colnames(prots))]
protsLFQ <- readSingleCellExperiment(protsLFQ,
ecol = grep("^LFQ.", colnames(protsLFQ)),
fnames = "Protein.IDs")
colnames(protsLFQ) <- gsub("LFQ.intensity.", "", colnames(protsLFQ))
## 3. iBAQ
protsIBAQ <- prots[, !grepl("^LFQ|^Intensity", colnames(prots))]
protsIBAQ <- readSingleCellExperiment(protsIBAQ,
ecol = grep("^iBAQ.", colnames(protsIBAQ)),
fnames = "Protein.IDs")
colnames(protsIBAQ) <- gsub("iBAQ.", "", colnames(protsIBAQ))
####---- Create the QFeatures object ----####
el <- ExperimentList(peptides = peps,
proteins_intensity = protsInt,
proteins_LFQ = protsLFQ,
proteins_iBAQ = protsIBAQ)
zhu2018NC_hela <- QFeatures(el, colData = annot)
## Create assay links
zhu2018NC_hela <- addAssayLink(zhu2018NC_hela,
from = "peptides", to = "proteins_intensity",
varFrom = "Leading.razor.protein",
varTo = "Majority.protein.IDs")
zhu2018NC_hela <- addAssayLink(zhu2018NC_hela,
from = "peptides", to = "proteins_LFQ",
varFrom = "Leading.razor.protein",
varTo = "Majority.protein.IDs")
zhu2018NC_hela <- addAssayLink(zhu2018NC_hela,
from = "peptides", to = "proteins_iBAQ",
varFrom = "Leading.razor.protein",
varTo = "Majority.protein.IDs")
# Save data as Rda file
# Note: saving is assumed to occur in "(...)/scpdata/inst/scripts"
save(zhu2018NC_hela,
file = "~/PhD/.localdata/scpdata/zhu2018NC_hela.Rda",
compress = "xz",
compression_level = 9)
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