groupComparisonPlots: Visualization for model-based analysis and summarizing...

In MSstats: Protein Significance Analysis in DDA, SRM and DIA for Label-free or Label-based Proteomics Experiments

Description

To summarize the results of log-fold changes and adjusted p-values for differentially abundant proteins, groupComparisonPlots takes testing results from function (groupComparison) as input and automatically generate three types of figures in pdf files as output : (1) volcano plot (specify "VolcanoPlot" in option type) for each comparison separately; (2) heatmap (specify "Heatmap" in option type) for multiple comparisons ; (3) comparison plot (specify "ComparisonPlot" in option type) for multiple comparisons per protein.

Usage

groupComparisonPlots(data=data,
		type=type,
		sig=0.05,
		FCcutoff=FALSE,
		logBase.pvalue=10,
		ylimUp=FALSE,
		ylimDown=FALSE,
		xlimUp=FALSE,
		x.axis.size=10,
		y.axis.size=10,
		dot.size=3,
		text.size=4,
		text.angle=0,
		legend.size=13,
		ProteinName=TRUE,
		colorkey=TRUE,
		numProtein=100, 
		clustering="both", 
		width=10, 
		height=10, 
		which.Comparison="all", 
		which.Protein="all",
		address="")

Arguments

data	'ComparisonResult' in testing output from function groupComparison.
type	choice of visualization. "VolcanoPlot" represents volcano plot of log fold changes and adjusted p-values for each comparison separately. "Heatmap" represents heatmap of adjusted p-values for multiple comparisons. "ComparisonPlot" represents comparison plot of log fold changes for multiple comparisons per protein.
sig	FDR cutoff for the adjusted p-values in heatmap and volcano plot. level of significance for comparison plot. 100(1-sig)% confidence interval will be drawn. sig=0.05 is default.
FCcutoff	for volcano plot or heatmap, whether involve fold change cutoff or not. FALSE (default) means no fold change cutoff is applied for significance analysis. FCcutoff = specific value means specific fold change cutoff is applied.
logBase.pvalue	for volcano plot or heatmap, (-) logarithm transformation of adjusted p-value with base 2 or 10(default).
ylimUp	for all three plots, upper limit for y-axis. FALSE (default) for volcano plot/heatmap use maximum of -log2 (adjusted p-value) or -log10 (adjusted p-value). FALSE (default) for comparison plot uses maximum of log-fold change + CI.
ylimDown	for all three plots, lower limit for y-axis. FALSE (default) for volcano plot/heatmap use minimum of -log2 (adjusted p-value) or -log10 (adjusted p-value). FALSE (default) for comparison plot uses minimum of log-fold change - CI.
xlimUp	for Volcano plot, the limit for x-axis. FALSE (default) for use maximum for absolute value of log-fold change or 3 as default if maximum for absolute value of log-fold change is less than 3.
x.axis.size	size of axes labels, e.g. name of the comparisons in heatmap, and in comparison plot. Default is 10.
y.axis.size	size of axes labels, e.g. name of targeted proteins in heatmap. Default is 10.
dot.size	size of dots in volcano plot and comparison plot. Default is 3.
text.size	size of ProteinName label in the graph for Volcano Plot. Default is 4.
text.angle	angle of x-axis labels represented each comparison at the bottom of graph in comparison plot. Default is 0.
legend.size	size of legend for color at the bottom of volcano plot. Default is 7.
ProteinName	for volcano plot only, whether display protein names or not. TRUE (default) means protein names, which are significant, are displayed next to the points. FALSE means no protein names are displayed.
colorkey	TRUE(default) shows colorkey.
numProtein	The number of proteins which will be presented in each heatmap. Default is 100. Maximum possible number of protein for one heatmap is 180.
clustering	Determines how to order proteins and comparisons. Hierarchical cluster analysis with Ward method(minimum variance) is performed. 'protein' means that protein dendrogram is computed and reordered based on protein means (the order of row is changed). 'comparison' means comparison dendrogram is computed and reordered based on comparison means (the order of comparison is changed). 'both' means to reorder both protein and comparison. Default is 'protein'.
width	width of the saved file. Default is 10.
height	height of the saved file. Default is 10.
which.Comparison	list of comparisons to draw plots. List can be labels of comparisons or order numbers of comparisons from levels(data$Label), such as levels(testResultMultiComparisons$ComparisonResult$Label). Default is "all", which generates all plots for each protein.
which.Protein	Protein list to draw comparison plots. List can be names of Proteins or order numbers of Proteins from levels(testResultMultiComparisons$ComparisonResult$Protein). Default is "all", which generates all comparison plots for each protein.
address	the name of folder that will store the results. Default folder is the current working directory. The other assigned folder has to be existed under the current working directory. An output pdf file is automatically created with the default name of "VolcanoPlot.pdf" or "Heatmap.pdf" or "ComparisonPlot.pdf". The command address can help to specify where to store the file as well as how to modify the beginning of the file name. If address=FALSE, plot will be not saved as pdf file but showed in window.

Details

• Volcano plot : illustrate actual log-fold changes and adjusted p-values for each comparison separately with all proteins. The x-axis is the log fold change. The base of logarithm transformation is the same as specified in "logTrans" from dataProcess. The y-axis is the negative log2 or log10 adjusted p-values. The horizontal dashed line represents the FDR cutoff. The points below the FDR cutoff line are non-significantly abundant proteins (colored in black). The points above the FDR cutoff line are significantly abundant proteins (colored in red/blue for up-/down-regulated). If fold change cutoff is specified (FCcutoff = specific value), the points above the FDR cutoff line but within the FC cutoff line are non-significantly abundant proteins (colored in black)/

• Heatmap : illustrate up-/down-regulated proteins for multiple comparisons with all proteins. Each column represents each comparison of interest. Each row represents each protein. Color red/blue represents proteins in that specific comparison are significantly up-regulated/down-regulated proteins with FDR cutoff and/or FC cutoff. The color scheme shows the evidences of significance. The darker color it is, the stronger evidence of significance it has. Color gold represents proteins are not significantly different in abundance.

• Comparison plot : illustrate log-fold change and its variation of multiple comparisons for single protein. X-axis is comparison of interest. Y-axis is the log fold change. The red points are the estimated log fold change from the model. The blue error bars are the confidence interval with 0.95 significant level for log fold change. This interval is only based on the standard error, which is estimated from the model.

The input of this function is "ComparisonResult" in the testing results from function (groupComparison).

Value

pdf file

Author(s)

Meena Choi, Olga Vitek.

Maintainer: Meena Choi ([e-mail])

References

Meena Choi, Ching-Yun Chang, Timothy Clough, Daniel Broudy, Trevor Killeen, Brendan MacLean and Olga Vitek. "MSstats: an R package for statistical analysis of quantitative mass spectrometry-based proteomic experiments" Bioinformatics, 30(17):2524-2526, 2014.

Ching-Yun Chang, Paola Picotti, Ruth Huttenhain, Viola Heinzelmann-Schwarz, Marko Jovanovic, Ruedi Aebersold, Olga Vitek. "Protein significance analysis in selected reaction monitoring (SRM) measurements." Molecular & Cellular Proteomics, 11:M111.014662, 2012.

Timothy Clough, Safia Thaminy, Susanne Ragg, Ruedi Aebersold, Olga Vitek. "Statistical protein quantification and significance analysis in label-free LC-M experiments with complex designs" BMC Bioinformatics, 13:S16, 2012.

Examples

QuantData<-dataProcess(SRMRawData)
head(QuantData$ProcessedData)

## based on multiple comparisons  (T1 vs T3; T1 vs T7; T1 vs T9)
comparison1<-matrix(c(-1,0,1,0,0,0,0,0,0,0),nrow=1)
comparison2<-matrix(c(-1,0,0,0,0,0,1,0,0,0),nrow=1)
comparison3<-matrix(c(-1,0,0,0,0,0,0,0,1,0),nrow=1)
comparison<-rbind(comparison1,comparison2, comparison3)
row.names(comparison)<-c("T3-T1","T7-T1","T9-T1")

testResultMultiComparisons<-groupComparison(contrast.matrix=comparison,data=QuantData)

testResultMultiComparisons$ComparisonResult

# Volcano plot with FDR cutoff = 0.05 and no FC cutoff
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="VolcanoPlot",
logBase.pvalue=2, address="Ex1_")

# Volcano plot with FDR cutoff = 0.05, FC cutoff = 70, upper y-axis limit = 100, 
# and no protein name displayed
# FCcutoff=70 is for demonstration purpose
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="VolcanoPlot",
FCcutoff=70, logBase.pvalue=2, ylimUp=100, ProteinName=FALSE,address="Ex2_")

# Heatmap with FDR cutoff = 0.05
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="Heatmap", 
logBase.pvalue=2, address="Ex1_")

# Heatmap with FDR cutoff = 0.05 and FC cutoff = 70
# FCcutoff=70 is for demonstration purpose
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="Heatmap",
FCcutoff=70, logBase.pvalue=2, address="Ex2_")

# Comparison Plot
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="ComparisonPlot",
address="Ex1_")

# Comparison Plot
groupComparisonPlots(data=testResultMultiComparisons$ComparisonResult, type="ComparisonPlot",
ylimUp=8, ylimDown=-1, address="Ex2_")

MSstats documentation built on Feb. 28, 2021, 2:01 a.m.