DEqMS 1.24.0
DEqMS
builds on top of Limma
, a widely-used R package for microarray data
analysis (Smyth G. et al 2004), and improves it with proteomics data specific
properties, accounting for variance dependence on the number of quantified
peptides or PSMs for statistical testing of differential protein expression.
Limma assumes a common prior variance for all proteinss, the function
spectraCounteBayes
in DEqMS package estimate prior variance
for proteins quantified by different number of PSMs.
A documentation of all R functions available in DEqMS is detailed in the PDF reference manual on the DEqMS Bioconductor page.
#Load the package
library(DEqMS)
## Loading required package: ggplot2
## Loading required package: matrixStats
## Loading required package: limma
As an example, we analyzed a protemoics dataset (TMT10plex labelled) in which A431 cells (human epidermoid carcinoma cell line) were treated with three different miRNA mimics (Zhou Y. Et al Oncogene 2017). The raw MS data was searched with MS-GF+ (Kim et al Nat Communications 2016) and post processed with Percolator (Kall L. et al Nat Method 2007). A tabular text output of protein table filtered at 1% protein level FDR is used.
options(timeout = 1000)
url <- "https://ftp.ebi.ac.uk/pride-archive/2016/06/PXD004163/Yan_miR_Protein_table.flatprottable.txt"
download.file(url, destfile = "./miR_Proteintable.txt",method = "auto")
df.prot = read.table("miR_Proteintable.txt",stringsAsFactors = FALSE,
header = TRUE, quote = "", comment.char = "",sep = "\t")
# filter at 1% protein FDR and extract TMT quantifications
TMT_columns = seq(15,33,2)
dat = df.prot[df.prot$miR.FASP_q.value<0.01,TMT_columns]
rownames(dat) = df.prot[df.prot$miR.FASP_q.value<0.01,]$Protein.accession
# The protein dataframe is a typical protein expression matrix structure
# Samples are in columns, proteins are in rows
# use unique protein IDs for rownames
# to view the whole data frame, use the command View(dat)
If the protein table is relative abundance (ratios) or intensity values, Log2 transform the data. Systematic effects and variance components are usually assumed to be additive on log scale (Oberg AL. et al JPR 2008; Hill EG. et al JPR 2008).
dat.log = log2(dat)
#remove rows with NAs
dat.log = na.omit(dat.log)
Use boxplot to check if the samples have medians centered. if not, do median centering.
boxplot(dat.log,las=2,main="TMT10plex data PXD004163")
# Here the data is already median centered, we skip the following step.
# dat.log = equalMedianNormalization(dat.log)
A design table is used to tell how samples are arranged in different groups/classes.
# if there is only one factor, such as treatment. You can define a vector with
# the treatment group in the same order as samples in the protein table.
cond = as.factor(c("ctrl","miR191","miR372","miR519","ctrl",
"miR372","miR519","ctrl","miR191","miR372"))
# The function model.matrix is used to generate the design matrix
design = model.matrix(~0+cond) # 0 means no intercept for the linear model
colnames(design) = gsub("cond","",colnames(design))
In addition to the design, you need to define the contrast, which tells the model to compare the differences between specific groups. Start with the Limma part.
# you can define one or multiple contrasts here
x <- c("miR372-ctrl","miR519-ctrl","miR191-ctrl",
"miR372-miR519","miR372-miR191","miR519-miR191")
contrast = makeContrasts(contrasts=x,levels=design)
fit1 <- lmFit(dat.log, design)
fit2 <- contrasts.fit(fit1,contrasts = contrast)
fit3 <- eBayes(fit2)
The above shows Limma part, now we use the function spectraCounteBayes
in DEqMS to correct bias of variance estimate based on minimum number of
psms per protein used for quantification.We use the minimum number of PSMs
used for quantification within and across experiments to model the relation
between variance and PSM count.(See original paper)
# assign a extra variable `count` to fit3 object, telling how many PSMs are
# quantifed for each protein
library(matrixStats)
count_columns = seq(16,34,2)
psm.count.table = data.frame(count = rowMins(
as.matrix(df.prot[,count_columns])), row.names = df.prot$Protein.accession)
fit3$count = psm.count.table[rownames(fit3$coefficients),"count"]
fit4 = spectraCounteBayes(fit3)
Outputs of spectraCounteBayes
:
object is augmented form of “fit” object from eBayes
in Limma, with the
additions being:
sca.t
- Spectra Count Adjusted posterior t-value
sca.p
- Spectra Count Adjusted posterior p-value
sca.dfprior
- DEqMS estimated prior degrees of freedom
sca.priorvar
- DEqMS estimated prior variance
sca.postvar
- DEqMS estimated posterior variance
model
- fitted model
# n=30 limits the boxplot to show only proteins quantified by <= 30 PSMs.
VarianceBoxplot(fit4,n=30,main="TMT10plex dataset PXD004163",xlab="PSM count")
VarianceScatterplot(fit4,main="TMT10plex dataset PXD004163")
DEqMS.results = outputResult(fit4,coef_col = 1)
#if you are not sure which coef_col refers to the specific contrast,type
head(fit4$coefficients)
## Contrasts
## miR372-ctrl miR519-ctrl miR191-ctrl miR372-miR519 miR372-miR191
## A2M -0.49200598 -0.36004725 -0.29168559 -0.13195872 -0.2003203925
## AAAS -0.10579819 -0.16658093 -0.12904503 0.06078273 0.0232468358
## AACS -0.06426210 -0.01691172 -0.06517334 -0.04735038 0.0009112413
## AAED1 0.28361527 0.11312650 0.11297711 0.17048876 0.1706381600
## AAGAB 0.06942315 -0.02252727 0.18841027 0.09195042 -0.1189871230
## AAK1 0.01017744 0.19826414 -0.03174740 -0.18808671 0.0419248388
## Contrasts
## miR519-miR191
## A2M -0.0683616685
## AAAS -0.0375358970
## AACS 0.0482616247
## AAED1 0.0001493955
## AAGAB -0.2109375393
## AAK1 0.2300115440
# a quick look on the DEqMS results table
head(DEqMS.results)
## logFC AveExpr t P.Value adj.P.Val B
## ANKRD52 -1.2510508 -0.5579726 -22.87106 1.526501e-09 1.317828e-05 11.285532
## CROT -1.2470819 -0.4499388 -14.12934 1.237413e-07 3.560861e-04 8.042317
## PDCD4 -0.7673770 -0.2662663 -13.42734 1.954766e-07 4.218875e-04 7.652462
## ATAD2 -0.6719598 -0.4584266 -11.76618 6.328104e-07 5.129415e-04 6.614667
## RELA -0.6208005 -0.2296114 -12.08909 4.980318e-07 5.129415e-04 6.830220
## ZKSCAN1 -0.8846205 -0.5034830 -12.41816 3.924351e-07 5.129415e-04 7.042732
## gene count sca.t sca.P.Value sca.adj.pval
## ANKRD52 ANKRD52 17 -22.52489 2.604115e-11 2.248132e-07
## CROT CROT 22 -15.37439 2.364669e-09 1.020709e-05
## PDCD4 PDCD4 40 -14.40705 5.027631e-09 1.446785e-05
## ATAD2 ATAD2 51 -12.75244 2.042809e-08 4.074288e-05
## RELA RELA 32 -12.59211 2.359717e-08 4.074288e-05
## ZKSCAN1 ZKSCAN1 10 -12.15065 3.539633e-08 4.746132e-05
# Save it into a tabular text file
write.table(DEqMS.results,"DEqMS.results.miR372-ctrl.txt",sep = "\t",
row.names = F,quote=F)
Explaination of the columns in DEqMS.results
:
logFC
- log2 fold change between two groups, Here it’s log2(miR372/ctrl).
AveExpr
- the mean of the log2 ratios/intensities across all samples. Since
input matrix is log2 ratio values, it is the mean log2 ratios of all samples.
t
- Limma output t-statistics
P.Value
- Limma p-values
adj.P.Val
- BH method adjusted Limma p-values
B
- Limma B values
count
- PSM/peptide count values you assigned
sca.t
- DEqMS t-statistics
sca.P.Value
- DEqMS p-values
sca.adj.pval
- BH method adjusted DEqMS p-values
We recommend to plot p-values on y-axis instead of adjusted pvalue or FDR.
Read about why here.
library(ggrepel)
# Use ggplot2 allows more flexibility in plotting
DEqMS.results$log.sca.pval = -log10(DEqMS.results$sca.P.Value)
ggplot(DEqMS.results, aes(x = logFC, y =log.sca.pval )) +
geom_point(size=0.5 )+
theme_bw(base_size = 16) + # change theme
xlab(expression("log2(miR372/ctrl)")) + # x-axis label
ylab(expression(" -log10(P-value)")) + # y-axis label
geom_vline(xintercept = c(-1,1), colour = "red") + # Add fold change cutoffs
geom_hline(yintercept = 3, colour = "red") + # Add significance cutoffs
geom_vline(xintercept = 0, colour = "black") + # Add 0 lines
scale_colour_gradient(low = "black", high = "black", guide = FALSE)+
geom_text_repel(data=subset(DEqMS.results, abs(logFC)>1&log.sca.pval > 3),
aes( logFC, log.sca.pval ,label=gene)) # add gene label
## Warning: The `guide` argument in `scale_*()` cannot be `FALSE`. This was deprecated in
## ggplot2 3.3.4.
## ℹ Please use "none" instead.
## This warning is displayed once every 8 hours.
## Call `lifecycle::last_lifecycle_warnings()` to see where this warning was
## generated.
you can also use volcanoplot
function from Limma. However, it uses p.value
from Limma. If you want to plot sca.pvalue
from DEqMS, you need to modify the
fit4
object.
fit4$p.value = fit4$sca.p
# volcanoplot highlight top 20 proteins ranked by p-value here
volcanoplot(fit4,coef=1, style = "p-value", highlight = 20,
names=rownames(fit4$coefficients))
Here we analyze a published label-free benchmark dataset in which either 10 or 30 µg of E. coli protein extract was spiked into human protein extracts (50 µg) in triplicates (Cox J et al MCP 2014). The data was searched by MaxQuant software and the output file “proteinGroups.txt” was used here.
url2 <- "https://ftp.ebi.ac.uk/pride-archive/2014/09/PXD000279/proteomebenchmark.zip"
download.file(url2, destfile = "./PXD000279.zip",method = "auto")
unzip("PXD000279.zip")
df.prot = read.table("proteinGroups.txt",header=T,sep="\t",stringsAsFactors = F,
comment.char = "",quote ="")
# remove decoy matches and matches to contaminant
df.prot = df.prot[!df.prot$Reverse=="+",]
df.prot = df.prot[!df.prot$Contaminant=="+",]
# Extract columns of LFQ intensites
df.LFQ = df.prot[,89:94]
df.LFQ[df.LFQ==0] <- NA
rownames(df.LFQ) = df.prot$Majority.protein.IDs
df.LFQ$na_count_H = apply(df.LFQ,1,function(x) sum(is.na(x[1:3])))
df.LFQ$na_count_L = apply(df.LFQ,1,function(x) sum(is.na(x[4:6])))
# Filter protein table. DEqMS require minimum two values for each group.
df.LFQ.filter = df.LFQ[df.LFQ$na_count_H<2 & df.LFQ$na_count_L<2,1:6]
library(matrixStats)
# we use minimum peptide count among six samples
# count unique+razor peptides used for quantification
pep.count.table = data.frame(count = rowMins(as.matrix(df.prot[,19:24])),
row.names = df.prot$Majority.protein.IDs)
# Minimum peptide count of some proteins can be 0
# add pseudocount 1 to all proteins
pep.count.table$count = pep.count.table$count+1
protein.matrix = log2(as.matrix(df.LFQ.filter))
class = as.factor(c("H","H","H","L","L","L"))
design = model.matrix(~0+class) # fitting without intercept
fit1 = lmFit(protein.matrix,design = design)
cont <- makeContrasts(classH-classL, levels = design)
fit2 = contrasts.fit(fit1,contrasts = cont)
fit3 <- eBayes(fit2)
fit3$count = pep.count.table[rownames(fit3$coefficients),"count"]
#check the values in the vector fit3$count
#if min(fit3$count) return NA or 0, you should troubleshoot the error first
min(fit3$count)
## [1] 1
fit4 = spectraCounteBayes(fit3)
VarianceBoxplot(fit4, n=20, main = "Label-free dataset PXD000279",
xlab="peptide count + 1")
DEqMS.results = outputResult(fit4,coef_col = 1)
# Add Gene names to the data frame
rownames(df.prot) = df.prot$Majority.protein.IDs
DEqMS.results$Gene.name = df.prot[DEqMS.results$gene,]$Gene.names
head(DEqMS.results)
## logFC AveExpr t P.Value adj.P.Val B gene
## P0A8V2 1.290950 32.97213 11.894233 1.140801e-05 0.0005926658 4.148090 P0A8V2
## P07118 1.266198 30.78180 12.015511 1.070353e-05 0.0005926658 4.211194 P07118
## P0AFG3 1.335840 31.65885 12.668638 7.669201e-06 0.0005926658 4.538511 P0AFG3
## P09373 1.245161 35.04896 11.315078 1.559908e-05 0.0005926658 3.836067 P09373
## P27298 1.353797 31.18702 12.456539 8.530817e-06 0.0005926658 4.434473 P27298
## P0AFG8 1.065060 34.13384 9.831808 3.735319e-05 0.0006115825 2.947425 P0AFG8
## count sca.t sca.P.Value sca.adj.pval Gene.name
## P0A8V2 56 26.73381 2.450270e-10 8.944812e-07 rpoB
## P07118 38 24.92869 4.752226e-10 8.944812e-07 valS
## P0AFG3 33 24.62180 5.343376e-10 8.944812e-07 sucA
## P09373 41 22.37242 1.321228e-09 1.382583e-06 pflB
## P27298 30 22.27540 1.376526e-09 1.382583e-06 prlC
## P0AFG8 47 20.96849 2.433443e-09 1.999993e-06 aceE
write.table(DEqMS.results,"H-L.DEqMS.results.txt",sep = "\t",
row.names = F,quote=F)
If you want to try different methods to estimate protein abundance,you can
start with a PSM table and use provided functions in DEqMS to summarize PSM
quant data into protein quant data. Four different functions are included: medianSweeping
,medianSummary
,medpolishSummary
,farmsSummary
.
Check PDF reference manual for detailed description.
### retrieve example PSM dataset from ExperimentHub
library(ExperimentHub)
eh = ExperimentHub()
query(eh, "DEqMS")
## ExperimentHub with 4 records
## # snapshotDate(): 2024-10-24
## # $dataprovider: ProteomeXchange, Swedish BioMS infrastructure
## # $species: Homo sapiens, Saccharomyces cerevisiae
## # $rdataclass: data.frame
## # additional mcols(): taxonomyid, genome, description,
## # coordinate_1_based, maintainer, rdatadateadded, preparerclass, tags,
## # rdatapath, sourceurl, sourcetype
## # retrieve records with, e.g., 'object[["EH1663"]]'
##
## title
## EH1663 | microRNA treated A431 cell proteomics data
## EH7780 | microRNA treated A431 cell TMT10plex proteomics data-ProteinTable
## EH7781 | MaxQuant LFQ benchmark dataset
## EH7782 | DIA quantification UPS1 spike-in dataset
dat.psm = eh[["EH1663"]]
dat.psm.log = dat.psm
dat.psm.log[,3:12] = log2(dat.psm[,3:12])
head(dat.psm.log)
## Peptide gene tmt10plex_126
## 1 +229.163EK+229.163EDDEEEEDEDASGGDQDQEER RAD21 16.75237
## 2 +229.163LGLGIDEDEVAAEEPNAAVPDEIPPLEGDEDASR HSP90AB1 10.83812
## 3 +229.163TEGDEEAEEEQEENLEASGDYK+229.163 XRCC6 14.50514
## 4 +229.163GDAEK+229.163PEEELEEDDDEELDETLSER TOMM22 15.03117
## 8 +229.163APLATGEDDDDEVPDLVENFDEASK+229.163 BTF3 12.91406
## 9 +229.163LEEEDEDEEDGESGC+57.021TFLVGLIQK+229.163 CAPN2 14.98558
## tmt10plex_127N tmt10plex_127C tmt10plex_128N tmt10plex_128C tmt10plex_129N
## 1 16.58542 17.26731 16.89528 17.01872 17.57275
## 2 10.13673 11.11384 11.07480 10.94694 10.79556
## 3 14.24282 15.23424 14.89867 14.74940 14.97737
## 4 14.91910 15.41189 15.28130 15.28605 15.41345
## 8 12.95097 13.00558 13.42184 12.63930 13.62308
## 9 14.97605 15.30197 15.27980 15.10410 15.31982
## tmt10plex_129C tmt10plex_130N tmt10plex_130C tmt10plex_131
## 1 17.17815 16.86259 17.10233 17.75614
## 2 11.12758 11.14692 10.82071 11.21737
## 3 15.15130 15.09598 15.01059 15.46618
## 4 15.25668 15.39181 15.26238 15.79845
## 8 13.12886 12.19316 12.90018 13.52949
## 9 15.25234 15.51071 15.72660 16.06220
Here, median sweeping is used to summarize PSMs intensities to protein log2
ratios. In this procedure, we substract the spectrum log2 intensity from the
median log2 intensities of all samples. The relative abundance estimate for
each protein is calculated as the median over all PSMs belonging to this
protein.(Herbrich et al JPR 2012 and D’Angelo et al JPR 2016).
Assume the log2 intensity of PSM i
in sample j
is \(y_{i,j}\), its relative
log2 intensity of PSM i
in sample j
is \(y'_{i,j}\):
\[y'_{i,j} = y_{i,j} - median_{j'\in ctrl}\ y_{i,j'} \]
Relative abundance of protein k
in sample j
\(Y_{k,j}\) is calculated as:
\[Y_{k,j} = median_{i\in protein\ k}\ y'_{i,j} \]
Correction for differences in amounts of material loaded in the channels is then done by subtracting the channel median from the relative abundance (log2 ratio), centering all channels to have median log2 value of zero.
dat.gene.nm = medianSweeping(dat.psm.log,group_col = 2)
boxplot(dat.gene.nm,las=2,ylab="log2 ratio",main="TMT10plex dataset PXD004163")
gene.matrix = as.matrix(dat.gene.nm)
# make design table
cond = as.factor(c("ctrl","miR191","miR372","miR519","ctrl",
"miR372","miR519","ctrl","miR191","miR372"))
design = model.matrix(~0+cond)
colnames(design) = gsub("cond","",colnames(design))
#limma part analysis
fit1 <- lmFit(gene.matrix,design)
x <- c("miR372-ctrl","miR519-ctrl","miR191-ctrl")
contrast = makeContrasts(contrasts=x,levels=design)
fit2 <- eBayes(contrasts.fit(fit1,contrasts = contrast))
#DEqMS part analysis
psm.count.table = as.data.frame(table(dat.psm$gene))
rownames(psm.count.table) = psm.count.table$Var1
fit2$count = psm.count.table[rownames(fit2$coefficients),2]
fit3 = spectraCounteBayes(fit2)
# extract DEqMS results
DEqMS.results = outputResult(fit3,coef_col = 1)
head(DEqMS.results)
## logFC AveExpr t P.Value adj.P.Val B
## ANKRD52 -1.1917809 -0.093887723 -18.26692 2.608305e-08 0.0001326236 9.113399
## CROT -1.1997155 -0.060459201 -16.41503 6.530463e-08 0.0002000934 8.438659
## TGFBR2 -1.3474739 0.083901815 -18.05371 2.885630e-08 0.0001326236 9.041434
## PDCD4 -0.7800666 0.007360661 -13.07496 4.512500e-07 0.0008295781 6.874678
## TRPS1 -0.8122847 -0.050833888 -11.70281 1.142391e-06 0.0013126073 6.063183
## PHLPP2 -0.7969800 -0.001069459 -14.37066 2.029693e-07 0.0004664235 7.543032
## gene count sca.t sca.P.Value sca.adj.pval
## ANKRD52 ANKRD52 17 -18.97949 3.769162e-10 3.147509e-06
## CROT CROT 20 -17.59956 8.866593e-10 3.147509e-06
## TGFBR2 TGFBR2 7 -17.37181 1.027255e-09 3.147509e-06
## PDCD4 PDCD4 40 -14.25841 9.397591e-09 2.159566e-05
## TRPS1 TRPS1 30 -12.78539 3.133624e-08 4.919434e-05
## PHLPP2 PHLPP2 8 -12.75696 3.211119e-08 4.919434e-05
write.table(DEqMS.results,"DEqMS.results.miR372-ctrl.fromPSMtable.txt",
sep = "\t",row.names = F,quote=F)
Generate variance ~ PMS count boxplot, check if the DEqMS correctly find the relation between prior variance and PSM count
VarianceBoxplot(fit3,n=20, xlab="PSM count",main="TMT10plex dataset PXD004163")
Only possible if you read a PSM or peptide table as input.
peptideProfilePlot
function will plot log2 intensity of each PSM/peptide of
the protein in the input table.
peptideProfilePlot(dat=dat.psm.log,col=2,gene="TGFBR2")
## Using Peptide, gene as id variables
# col=2 is tell in which column of dat.psm.log to look for the gene
The following steps are not required for get the results from DEqMS. it is used to help users to understand the method better and the differences to other methods. Here we use the TMT labelled data PXD004163 as an example.
VarianceScatterplot(fit3, xlab="log2(PSM count)")
limma.prior = fit3$s2.prior
abline(h = log(limma.prior),col="green",lwd=3 )
legend("topright",legend=c("DEqMS prior variance","Limma prior variance"),
col=c("red","green"),lwd=3)
op <- par(mfrow=c(1,2), mar=c(4,4,4,1), oma=c(0.5,0.5,0.5,0))
Residualplot(fit3, xlab="log2(PSM count)",main="DEqMS")
x = fit3$count
y = log(limma.prior) - log(fit3$sigma^2)
plot(log2(x),y,ylim=c(-6,2),ylab="Variance(estimated-observed)", pch=20, cex=0.5,
xlab = "log2(PSMcount)",main="Limma")
The plot here shows posterior variance of proteins “shrink” toward the fitted value to different extent depending on PSM number.
library(LSD)
op <- par(mfrow=c(1,2), mar=c(4,4,4,1), oma=c(0.5,0.5,0.5,0))
x = fit3$count
y = fit3$s2.post
heatscatter(log2(x),log(y),pch=20, xlab = "log2(PSMcount)",
ylab="log(Variance)",
main="Posterior Variance in Limma")
y = fit3$sca.postvar
heatscatter(log2(x),log(y),pch=20, xlab = "log2(PSMcount)",
ylab="log(Variance)",
main="Posterior Variance in DEqMS")
We first apply t.test to detect significant protein changes between ctrl samples and miR372 treated samples, both have three replicates.
pval.372 = apply(dat.gene.nm, 1, function(x)
t.test(as.numeric(x[c(1,5,8)]), as.numeric(x[c(3,6,10)]))$p.value)
logFC.372 = rowMeans(dat.gene.nm[,c(3,6,10)])-rowMeans(dat.gene.nm[,c(1,5,8)])
Generate a data.frame of t.test results, add PSM count values and order the table by p-value.
ttest.results = data.frame(gene=rownames(dat.gene.nm),
logFC=logFC.372,P.Value = pval.372,
adj.pval = p.adjust(pval.372,method = "BH"))
ttest.results$PSMcount = psm.count.table[ttest.results$gene,"count"]
ttest.results = ttest.results[with(ttest.results, order(P.Value)), ]
head(ttest.results)
## gene logFC P.Value adj.pval
## CCNE2 CCNE2 0.5386427 6.522987e-07 0.00599593
## CPSF2 CPSF2 0.1077977 7.633799e-06 0.03508494
## PPOX PPOX -0.2464418 2.546510e-05 0.07802507
## RELA RELA -0.5617739 5.078761e-05 0.11670992
## IFIT1 IFIT1 0.6375060 7.300925e-05 0.13422020
## MAGEA6 MAGEA6 0.4625733 1.093648e-04 0.16178031
Anova analysis is equivalent to linear model analysis. The difference to Limma analysis is that estimated variance is not moderated using empirical bayesian approach as it is done in Limma.
ord.t = fit1$coefficients[, 1]/fit1$sigma/fit1$stdev.unscaled[, 1]
ord.p = 2*pt(abs(ord.t), fit1$df.residual, lower.tail = FALSE)
ord.q = p.adjust(ord.p,method = "BH")
anova.results = data.frame(gene=names(fit1$sigma),
logFC=fit1$coefficients[,1],
t=ord.t,
P.Value=ord.p,
adj.P.Val = ord.q)
anova.results$PSMcount = psm.count.table[anova.results$gene,"count"]
anova.results = anova.results[with(anova.results,order(P.Value)),]
head(anova.results)
## gene logFC t P.Value adj.P.Val
## IFIT1 IFIT1 -0.8608329 -21.42050 6.753255e-07 0.003817858
## GULP1 GULP1 -0.3007482 -20.68542 8.306916e-07 0.003817858
## HMGCS1 HMGCS1 -0.2647281 -16.89451 2.748573e-06 0.007115321
## MB21D2 MB21D2 -0.2322144 -16.55622 3.096310e-06 0.007115321
## DDX58 DDX58 -0.3693960 -15.79362 4.086084e-06 0.007511856
## PHLPP2 PHLPP2 0.4988921 14.57485 6.545069e-06 0.007954545
Extract limma results using topTable
function, coef = 1
allows you to
extract the specific contrast (miR372-ctrl), option n= Inf
output
all rows.
limma.results = topTable(fit2,coef = 1,n= Inf)
limma.results$gene = rownames(limma.results)
#Add PSM count values in the data frame
limma.results$PSMcount = psm.count.table[limma.results$gene,"count"]
head(limma.results)
## logFC AveExpr t P.Value adj.P.Val B
## ANKRD52 -1.1917809 -0.093887723 -18.26692 2.608305e-08 0.0001326236 9.113399
## TGFBR2 -1.3474739 0.083901815 -18.05371 2.885630e-08 0.0001326236 9.041434
## CROT -1.1997155 -0.060459201 -16.41503 6.530463e-08 0.0002000934 8.438659
## PHLPP2 -0.7969800 -0.001069459 -14.37066 2.029693e-07 0.0004664235 7.543032
## PDCD4 -0.7800666 0.007360661 -13.07496 4.512500e-07 0.0008295781 6.874678
## ZKSCAN1 -0.8816149 -0.056612793 -11.95070 9.591643e-07 0.0012877234 6.218545
## gene
## ANKRD52 ANKRD52
## TGFBR2 TGFBR2
## CROT CROT
## PHLPP2 PHLPP2
## PDCD4 PDCD4
## ZKSCAN1 ZKSCAN1
plotting all proteins ranked by p-values.
plot(sort(-log10(limma.results$P.Value),decreasing = TRUE),
type="l",lty=2,lwd=2, ylab="-log10(p-value)",ylim = c(0,10),
xlab="Proteins ranked by p-values",
col="purple")
lines(sort(-log10(DEqMS.results$sca.P.Value),decreasing = TRUE),
lty=1,lwd=2,col="red")
lines(sort(-log10(anova.results$P.Value),decreasing = TRUE),
lty=2,lwd=2,col="blue")
lines(sort(-log10(ttest.results$P.Value),decreasing = TRUE),
lty=2,lwd=2,col="orange")
legend("topright",legend = c("Limma","DEqMS","Anova","t.test"),
col = c("purple","red","blue","orange"),lty=c(2,1,2,2),lwd=2)
plotting top 500 proteins ranked by p-values.
plot(sort(-log10(limma.results$P.Value),decreasing = TRUE)[1:500],
type="l",lty=2,lwd=2, ylab="-log10(p-value)", ylim = c(2,10),
xlab="Proteins ranked by p-values",
col="purple")
lines(sort(-log10(DEqMS.results$sca.P.Value),decreasing = TRUE)[1:500],
lty=1,lwd=2,col="red")
lines(sort(-log10(anova.results$P.Value),decreasing = TRUE)[1:500],
lty=2,lwd=2,col="blue")
lines(sort(-log10(ttest.results$P.Value),decreasing = TRUE)[1:500],
lty=2,lwd=2,col="orange")
legend("topright",legend = c("Limma","DEqMS","Anova","t.test"),
col = c("purple","red","blue","orange"),lty=c(2,1,2,2),lwd=2)