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Evaluate the effect of centering & scaling

1-correlation distance

Effect of centering and scaling on clustering of genes and samples in terms of distance. 'Yes' means the distance was changed compared to the baseline where no centering or scaling was applied.

clustering genes clustering samples
centering on each genes No Yes*
scaling on each genes No Yes*
  • Note: Cor(X, Y) = Cor(X + constant scalar, Y). If the constant is not a scalar, the equation won't hold. Or think about plotting data in a 2 dimension space. If the X data has a constant shift for all observations/genes, then the linear correlation won't be changed.

Euclidean distance

clustering genes clustering samples
centering on each genes Yes No1
scaling on each genes Yes Yes2

Note

  1. [math]\displaystyle{ \sum(X_i - Y_i)^2 = \sum(X_i-c_i - (Y_i-c_i))^2 }[/math]
  2. [math]\displaystyle{ \sum(X_i - Y_i)^2 \neq \sum(X_i/c_i - Y_i/c_i)^2 }[/math]

Supporting R code

1. 1-Corr distance

source("http://www.bioconductor.org/biocLite.R")
biocLite("limma"); biocLite("ALL")

library(limma); library(ALL)
data(ALL)

eset <- ALL[, ALL$mol.biol %in% c("BCR/ABL", "ALL1/AF4")]

f <- factor(as.character(eset$mol.biol))
design <- model.matrix(~f)
fit <- eBayes(lmFit(eset,design))
selected  <- p.adjust(fit$p.value[, 2]) < 0.05
esetSel <- eset [selected, ]   # 165 x 47
heatmap(exprs(esetSel))

esetSel2 <- esetSel[sample(1:nrow(esetSel), 20), sample(1:ncol(esetSel), 10)] # 20 x 10

dist.no <- 1-cor(t(as.matrix(esetSel2))) 
dist.mean <- 1-cor(t(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2))))) # gene variance has not changed!
dist.median <- 1-cor(t(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median))))

range(dist.no - dist.mean) # [1] -1.110223e-16  0.000000e+00
range(dist.no - dist.median) # [1] -1.110223e-16  0.000000e+00
range(dist.mean - dist.median) # [1] 0 0

So centering (no matter which measure: mean, median, ...) genes won't affect 1-corr distance of genes.

dist.mean <- 1-cor(t(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)), "/")))
dist.median <- 1-cor(t(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median), "/")))
range(dist.no - dist.mean) # [1] -8.881784e-16  6.661338e-16
range(dist.no - dist.median) # [1] -6.661338e-16  6.661338e-16
range(dist.mean - dist.median) # [1] -1.110223e-15  1.554312e-15

So scaling after centering (no matter what measures: mean, median,...) won't affect 1-corr distance of genes.

How about centering / scaling genes on array clustering?

dist.no <- 1-cor(as.matrix(esetSel2))
dist.mean <- 1-cor(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)))) # array variance has changed!
dist.median <- 1-cor(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median)))

range(dist.no - dist.mean) # [1] -1.547086  0.000000
range(dist.no - dist.median) # [1] -1.483427  0.000000
range(dist.mean - dist.median) # [1] -0.5283601  0.6164602

dist.mean <- 1-cor(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)), "/"))
dist.median <- 1-cor(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median), "/"))
range(dist.no - dist.mean) # [1] -1.477407  0.000000
range(dist.no - dist.median) # [1] -1.349419  0.000000
range(dist.mean - dist.median) # [1] -0.5419534  0.6269875

2. Euclidean distance

dist.no <- dist(as.matrix(esetSel2))
dist.mean <- dist(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2))))
dist.median <- dist(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median)))

range(dist.no - dist.mean) # [1] 7.198864e-05 2.193487e+01
range(dist.no - dist.median) # [1] -0.3715231 21.9320846
range(dist.mean - dist.median) # [1] -0.923717629 -0.000088385

Centering does affect the Euclidean distance.

dist.mean <- dist(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)), "/"))
dist.median <- dist(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median), "/"))

range(dist.no - dist.mean) # [1]  0.7005071 24.0698991
range(dist.no - dist.median) # [1]  0.636749 24.068920
range(dist.mean - dist.median) # [1] -0.22122869  0.02906131

And scaling affects Euclidean distance too.

How about centering / scaling genes on array clustering?

dist.no <- dist(t(as.matrix(esetSel2)))
dist.mean <- dist(t(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)))))
dist.median <- dist(t(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median))))

range(dist.no - dist.mean) # 0 0
range(dist.no - dist.median)  # 0 0
range(dist.mean - dist.median) # 0 0

dist.mean <- dist(t(sweep(as.matrix(esetSel2), 1L, rowMeans(as.matrix(esetSel2)), "/")))
dist.median <- dist(t(sweep(as.matrix(esetSel2), 1L, apply(esetSel2, 1, median), "/")))

range(dist.no - dist.mean) # [1] 1.698960 9.383789
range(dist.no - dist.median)  # [1] 1.683028 9.311603
range(dist.mean - dist.median) # [1] -0.09139173  0.02546394

Simple image plot using image() function

https://chitchatr.wordpress.com/2010/07/01/matrix-plots-in-r-a-neat-way-to-display-three-variables/

Simpleimage.png Simpleimage2.png

### Create Matrix plot using colors to fill grid
# Create matrix.   Using random values for this example.
rand <- rnorm(286, 0.8, 0.3)
mat <- matrix(sort(rand), nr=26)
dim(mat)  # Check dimensions
 
# Create x and y labels
yLabels <- seq(1, 26, 1)
xLabels <- c("a", "b", "c", "d", "e", "f", "g", "h", "i",
"j", "k");
 
# Set min and max values of rand
 min <- min(rand, na.rm=T)
 max <- max(rand, na.rm=T)
 
# Red and green range from 0 to 1 while Blue ranges from 1 to 0
 ColorRamp <- rgb(seq(0.95,0.99,length=50),  # Red
                  seq(0.95,0.05,length=50),  # Green
                  seq(0.95,0.05,length=50))  # Blue
 ColorLevels <- seq(min, max, length=length(ColorRamp))
 
# Set layout.  We are going to include a colorbar next to plot.
layout(matrix(data=c(1,2), nrow=1, ncol=2), widths=c(4,1),
         heights=c(1,1))
#plotting margins.  These seem to work well for me.
par(mar = c(5,5,2.5,1), font = 2)
 
# Plot it up!
image(1:ncol(mat), 1:nrow(mat), t(mat),
     col=ColorRamp, xlab="Variable", ylab="Time",
     axes=FALSE, zlim=c(min,max),
     main= NA)
 
# Now annotate the plot
box()
axis(side = 1, at=seq(1,length(xLabels),1), labels=xLabels,
      cex.axis=1.0)
axis(side = 2, at=seq(1,length(yLabels),1), labels=yLabels, las= 1,
      cex.axis=1)
 
# Add colorbar to second plot region
par(mar = c(3,2.5,2.5,2))
 image(1, ColorLevels,
      matrix(data=ColorLevels, ncol=length(ColorLevels),nrow=1),
      col=ColorRamp,xlab="",ylab="",xaxt="n", las = 1)

If we define ColorRamp variable using the following way, we will get the 2nd plot.

require(RColorBrewer) # get brewer.pal()
ColorRamp <- colorRampPalette( rev(brewer.pal(9, "RdBu")) )(25)

Note that

  • colorRampPalette() is an R's built-in function. It interpolate a set of given colors to create new color palettes. The return is a function that takes an integer argument (the required number of colors) and returns a character vector of colors (see rgb()) interpolating the given sequence (similar to heat.colors() or terrain.colors()).
# An example of showing 50 shades of grey in R
greys <- grep("^grey", colours(), value = TRUE)
length(greys)
# [1] 102
shadesOfGrey <- colorRampPalette(c("grey0", "grey100"))
shadesOfGrey(2)
# [1] "#000000" "#FFFFFF"
# And 50 shades of grey?
fiftyGreys <- shadesOfGrey(50)
mat <- matrix(rep(1:50, each = 50))
image(mat, axes = FALSE, col = fiftyGreys)
box()
  • brewer.pal(9, "RdBu") creates a diverging palette based on "RdBu" with 9 colors. See help(brewer.pal, package="RColorBrewer") for a list of palette name. The meaning of the palette name can be found on colorbrew2.org website.

gplots package

The following example is extracted from DESeq2 package.

Heatmap deseq2.png

## ----loadDESeq2, echo=FALSE----------------------------------------------
# in order to print version number below
library("DESeq2")

## ----loadExonsByGene, echo=FALSE-----------------------------------------
library("parathyroidSE")
library("GenomicFeatures")
data(exonsByGene)

## ----locateFiles, echo=FALSE---------------------------------------------
bamDir <- system.file("extdata",package="parathyroidSE",mustWork=TRUE)
fls <- list.files(bamDir, pattern="bam$",full=TRUE)


## ----bamfilepaired-------------------------------------------------------
library( "Rsamtools" )
bamLst <- BamFileList( fls, yieldSize=100000 )


## ----sumOver-------------------------------------------------------------
library( "GenomicAlignments" )
se <- summarizeOverlaps( exonsByGene, bamLst,
                         mode="Union",
                         singleEnd=FALSE,
                         ignore.strand=TRUE,
                         fragments=TRUE )

## ----libraries-----------------------------------------------------------
library( "DESeq2" )
library( "parathyroidSE" )

## ----loadEcs-------------------------------------------------------------
data( "parathyroidGenesSE" )
se <- parathyroidGenesSE
colnames(se) <- se$run

## ----fromSE--------------------------------------------------------------
ddsFull <- DESeqDataSet( se, design = ~ patient + treatment )

## ----collapse------------------------------------------------------------
ddsCollapsed <- collapseReplicates( ddsFull,
                                    groupby = ddsFull$sample, 
                                    run = ddsFull$run )

## ----subsetCols----------------------------------------------------------
dds <- ddsCollapsed[ , ddsCollapsed$time == "48h" ]

## ----subsetRows, echo=FALSE----------------------------------------------
idx <- which(rowSums(counts(dds)) > 0)[1:4000]
dds <- dds[idx,]

## ----runDESeq, cache=TRUE------------------------------------------------
dds <- DESeq(dds)

rld <- rlog( dds)

library( "genefilter" )
topVarGenes <- head( order( rowVars( assay(rld) ), decreasing=TRUE ), 35 )

## ----beginner_geneHeatmap, fig.width=9, fig.height=9---------------------
library(RColorBrewer)
library(gplots)
heatmap.2( assay(rld)[ topVarGenes, ], scale="row", 
           trace="none", dendrogram="column", 
           col = colorRampPalette( rev(brewer.pal(9, "RdBu")) )(255))

ggplot2 package

NMF package

aheatmap() function.

ComplexHeatmap

  • Groups of heatmaps
  • The color argument can contain a mapping function or a vector of colors. The circlize package (from the same package author) can be used.

Pros

pheatmap

(what is special?)

fheatmap

(archived)

corrplot

This package is used for visualization of correlation matrix. See its vignette and Visualize correlation matrix using correlogram.

Interactive heatmaps

d3heatmap

The package let you

  • Highlight rows/columns by clicking axis labels
  • Click and drag over colormap to zoom in (click on colormap to zoom out)
  • Optional clustering and dendrograms, courtesy of base::heatmap

heatmaply

This package extends the plotly engine to heatmaps, allowing you to inspect certain values of the data matrix by hovering the mouse over a cell. You can also zoom into a region of the heatmap by drawing a rectangle over an area of your choice.

Installing this package requires to compile some dependent package.

The return object is heatmaply is 'plotly' and 'htmlwidget'. It does not return the ordering of rows/columns. It can not control whether to do clustering (d3heatmap package is better at this).

canvasXpress

Colors

A quick introduction to using color in density plots

http://sharpsightlabs.com/blog/quick-intro-color-density-plot/

display.brewer.pal() and brewer.pal() functions

While brewer.pal() will return colors (in hex) for a certain palette, display.brew.pal() can display the colors on a graphical device.

library(RColorBrewer)
display.brewer.pal(11, "BrBG") # Alternative colors used in correlation matrix

display.brewer.pal(9, "Set1") # Up to 9 classes are allowed

Papers

Healthcare Access and Quality Index - Lancet

http://www.thelancet.com/pdfs/journals/lancet/PIIS0140-6736(17)30818-8.pdf