wmwTest.RdWe have implemented a highly efficient Wilcoxon-Mann-Whitney rank sum
test for high-throughput expression profiling data. For datasets with
more than 100 features (genes), the function can be more than 1,000
times faster than its R implementations (wilcox.test in
stats, or rankSumTestWithCorrelation in limma).
wmwTest( x, indexList, col = "GeneSymbol", valType = c("p.greater", "p.less", "p.two.sided", "U", "abs.log10p.greater", "log10p.less", "abs.log10p.two.sided", "Q"), simplify = TRUE ) # S4 method for matrix,IndexList wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for numeric,IndexList wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for matrix,GmtList wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for eSet,GmtList wmwTest( x, indexList, col = "GeneSymbol", valType = "p.greater", simplify = TRUE ) # S4 method for eSet,numeric wmwTest( x, indexList, col = "GeneSymbol", valType = "p.greater", simplify = TRUE ) # S4 method for eSet,logical wmwTest( x, indexList, col = "GeneSymbol", valType = "p.greater", simplify = TRUE ) # S4 method for eSet,list wmwTest( x, indexList, col = "GeneSymbol", valType = "p.greater", simplify = TRUE ) # S4 method for ANY,numeric wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for ANY,logical wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for ANY,list wmwTest(x, indexList, valType = "p.greater", simplify = TRUE) # S4 method for matrix,SignedIndexList wmwTest(x, indexList, valType, simplify = TRUE) # S4 method for matrix,SignedGenesets wmwTest(x, indexList, valType, simplify = TRUE) # S4 method for numeric,SignedIndexList wmwTest(x, indexList, valType, simplify = TRUE) # S4 method for eSet,SignedIndexList wmwTest(x, indexList, valType, simplify = TRUE) # S4 method for eSet,SignedGenesets wmwTest( x, indexList, col = "GeneSymbol", valType = c("p.greater", "p.less", "p.two.sided", "U", "abs.log10p.greater", "log10p.less", "abs.log10p.two.sided", "Q"), simplify = TRUE )
| x | A numeric matrix. All other data types (e.g. numeric vectors
or |
|---|---|
| indexList | A list of integer indices (starting from 1) indicating
signature genes. Can be of length zero. Other data types (e.g. a list
of numeric or logical vectors, or a numeric or logical vector) are
coerced into such a list. See |
| col | a string sometimes used with a |
| valType | The value type to be returned, allowed values
include |
| simplify | Logical. If not, the returning value is in matrix
format; if set to |
A numeric matrix or vector containing the statistic.
The basic application of the function is to test the enrichment of gene sets in expression profiling data or differentially expressed data (the matrix with feature/gene in rows and samples in columns).
A special case is when x is an eSet object
(e.g. ExpressionSet), and indexList is a list returned
from readGmt function. In this case, the only requirement is
that one column named GeneSymbol in the featureData
contain gene symbols used in the GMT file. The same applies to signed Gmt files. See the example below.
Besides the conventional value types such as ‘p.greater’,
‘p.less’, ‘p.two.sided’ , and ‘U’ (the U-statistic),
wmwTest (from version 0.99-1) provides further value types:
abs.log10p.greater and log10p.less perform log10
transformation on respective p-values and give the
transformed value a proper sign (positive for greater than, and
negative for less than); abs.log10p.two.sided transforms
two-sided p-values to non-negative values; and Q score
reports absolute log10-transformation of p-value of the
two-side variant, and gives a proper sign to it, depending on whether it is
rather greater than (positive) or less than (negative).
From version 1.19.1, the rank-biserial correlation coefficient (‘r’) and the common language effect size (‘f’) are supported value types.
x = matrix,indexList = IndexList: x is a matrix and indexList is a IndexList
x = numeric,indexList = IndexList: x is a numeric and indexList is a IndexList
x = matrix,indexList = GmtList: x is a matrix and indexList is a GmtList
x = eSet,indexList = GmtList: x is a eSet and indexList is a GmtList
x = eSet,indexList = numeric: x is a eSet and indexList is a numeric
x = eSet,indexList = logical: x is a eSet and indexList is a logical
x = eSet,indexList = list: x is a eSet and indexList is a list
x = ANY,indexList = numeric: x is ANY and indexList is a numeric
x = ANY,indexList = logical: x is ANY and indexList is a logical
x = ANY,indexList = list: x is ANY and indexList is a list
x = matrix,indexList = SignedIndexList: x is a matrix and indexList is a
SignedIndexList
x = matrix,indexList = SignedGenesets: x is a eSet and indexList is a
SignedIndexList
x = numeric,indexList = SignedIndexList: x is a numeric and indexList is a
SignedIndexList
x = eSet,indexList = SignedIndexList: x is a eSet and indexList is a
SignedIndexList
x = eSet,indexList = SignedGenesets: x is a eSet and indexList is a
SignedIndexList
The function has been optimized for expression profiling data. It
avoids repetitive ranking of data as done by native R implementations
and uses efficient C code to increase the performance and control
memory use. Simulation studies using expression profiles of 22000
genes in 2000 samples and 200 gene sets suggested that the C
implementation can be >1000 times faster than the R
implementation. And it is possible to further accelerate by
parallel calling the function with mclapply in the multicore package.
Barry, W.T., Nobel, A.B., and Wright, F.A. (2008). A statistical framework for testing functional namespaces in microarray data. _Annals of Applied Statistics_ 2, 286-315.
Wu, D, and Smyth, GK (2012). Camera: a competitive gene set test accounting for inter-gene correlation. _Nucleic Acids Research_ 40(17):e133
Zar, JH (1999). _Biostatistical Analysis 4th Edition_. Prentice-Hall International, Upper Saddle River, New Jersey.
codewilcox.test in the stats package, and rankSumTestWithCorrelation in
the limma package.
Jitao David Zhang <jitao_david.zhang@roche.com>
## R-native data structures set.seed(1887) rd <- rnorm(1000) rl <- sample(c(TRUE, FALSE), 1000, replace=TRUE) wmwTest(rd, rl, valType="p.two.sided")#> [1] 0.8535404#> [1] 0.8535404#> [1] 1.949087e-14wmwTest(rd1, rl, valType="U")#> [1] 90452#> [1] 0.9976222wmwTest(rd2, rl, valType="p.two.sided")#> [1] 0.004758899wmwTest(rd2, rl, valType="p.less")#> [1] 0.002379449wmwTest(rd2, rl, valType="r")#> [1] 0.1031357wmwTest(rd2, rl, valType="f")#> [1] 0.5515679## matrix forms rmat <- matrix(c(rd, rd1, rd2), ncol=3, byrow=FALSE) wmwTest(rmat, rl, valType="p.two.sided")#> [1] 8.535404e-01 3.898175e-14 4.758899e-03wmwTest(rmat, rl, valType="p.greater")#> [1] 4.267702e-01 1.949087e-14 9.976222e-01#> [1] 8.535404e-01 3.898175e-14 4.758899e-03#> [1] 4.267702e-01 1.949087e-14 9.976222e-01#> [1] 124152 90452 137887#> [1] 0.369805934 13.710168669 0.001033906#> [1] -2.416062e-01 -8.437865e-15 -2.623524e+00#> [1] 0.06877594 13.40913867 2.32249352#> [1] 0.06877594 13.40913867 -2.32249352#> [1] -0.006748243 -0.276357949 0.103135713#> [1] 0.4966259 0.3618210 0.5515679## using ExpressionSet data(sample.ExpressionSet) testSet <- sample.ExpressionSet fData(testSet)$GeneSymbol <- paste("GENE_",1:nrow(testSet), sep="") mySig1 <- sample(c(TRUE, FALSE), nrow(testSet), prob=c(0.25, 0.75), replace=TRUE) wmwTest(testSet, which(mySig1), valType="p.greater")#> A B C D E F G H #> 0.3968848 0.4750041 0.4090897 0.5238279 0.5757461 0.4790929 0.4343313 0.6157803 #> I J K L M N O P #> 0.6872272 0.5165239 0.4499611 0.5820556 0.4755881 0.4934181 0.4666891 0.4785086 #> Q R S T U V W X #> 0.6280457 0.2976157 0.3232340 0.6152199 0.6149396 0.3576255 0.3540736 0.4102298 #> Y Z #> 0.5086293 0.4288550## using integer exprs(testSet)[,1L] <- exprs(testSet)[,1L] + ifelse(mySig1, 50, 0) wmwTest(testSet, which(mySig1), valType="p.greater")#> A B C D E F #> 4.427725e-06 4.750041e-01 4.090897e-01 5.238279e-01 5.757461e-01 4.790929e-01 #> G H I J K L #> 4.343313e-01 6.157803e-01 6.872272e-01 5.165239e-01 4.499611e-01 5.820556e-01 #> M N O P Q R #> 4.755881e-01 4.934181e-01 4.666891e-01 4.785086e-01 6.280457e-01 2.976157e-01 #> S T U V W X #> 3.232340e-01 6.152199e-01 6.149396e-01 3.576255e-01 3.540736e-01 4.102298e-01 #> Y Z #> 5.086293e-01 4.288550e-01## using lists mySig2 <- sample(c(TRUE, FALSE), nrow(testSet), prob=c(0.6, 0.4), replace=TRUE) wmwTest(testSet, list(first=mySig1, second=mySig2))#> A B C D E F G #> first 4.427725e-06 0.4750041 0.4090897 0.5238279 0.5757461 0.4790929 0.4343313 #> second 3.322462e-01 0.5830970 0.4508703 0.4503638 0.4788279 0.2795935 0.5079108 #> H I J K L M N #> first 0.6157803 0.6872272 0.5165239 0.4499611 0.5820556 0.4755881 0.4934181 #> second 0.5554548 0.6009788 0.5637822 0.4024829 0.4129130 0.5557076 0.4844365 #> O P Q R S T U #> first 0.4666891 0.4785086 0.6280457 0.2976157 0.3232340 0.6152199 0.6149396 #> second 0.5477364 0.5394920 0.4508703 0.5673067 0.4577155 0.4478326 0.4821416 #> V W X Y Z #> first 0.3576255 0.3540736 0.4102298 0.5086293 0.4288550 #> second 0.3385415 0.6612245 0.5985069 0.6346372 0.3837895## using GMT file gmt_file <- system.file("extdata/exp.tissuemark.affy.roche.symbols.gmt", package="BioQC") gmt_list <- readGmt(gmt_file) gss <- sample(unlist(sapply(gmt_list, function(x) x$genes)), 1000) eset<-new("ExpressionSet", exprs=matrix(rnorm(10000), nrow=1000L), phenoData=new("AnnotatedDataFrame", data.frame(Sample=LETTERS[1:10])), featureData=new("AnnotatedDataFrame",data.frame(GeneSymbol=gss))) esetWmwRes <- wmwTest(eset ,gmt_list, valType="p.greater") summary(esetWmwRes)#> 1 2 3 4 #> Min. :0.02198 Min. :0.01316 Min. :0.005433 Min. :0.007333 #> 1st Qu.:0.28609 1st Qu.:0.24582 1st Qu.:0.194880 1st Qu.:0.233636 #> Median :0.55866 Median :0.51048 Median :0.460976 Median :0.598480 #> Mean :0.55896 Mean :0.50834 Mean :0.470506 Mean :0.547411 #> 3rd Qu.:0.79758 3rd Qu.:0.72584 3rd Qu.:0.706622 3rd Qu.:0.848243 #> Max. :1.00000 Max. :1.00000 Max. :1.000000 Max. :1.000000 #> 5 6 7 8 #> Min. :0.002327 Min. :0.01225 Min. :0.00879 Min. :0.0002731 #> 1st Qu.:0.262446 1st Qu.:0.27261 1st Qu.:0.23966 1st Qu.:0.2535412 #> Median :0.531550 Median :0.58203 Median :0.52827 Median :0.5691982 #> Mean :0.523777 Mean :0.55246 Mean :0.52780 Mean :0.5251984 #> 3rd Qu.:0.773279 3rd Qu.:0.79958 3rd Qu.:0.80507 3rd Qu.:0.7977362 #> Max. :1.000000 Max. :1.00000 Max. :1.00000 Max. :1.0000000 #> 9 10 #> Min. :0.001639 Min. :0.009709 #> 1st Qu.:0.265712 1st Qu.:0.273843 #> Median :0.503677 Median :0.517334 #> Mean :0.513945 Mean :0.531123 #> 3rd Qu.:0.738335 3rd Qu.:0.817494 #> Max. :1.000000 Max. :1.000000## using signed GMT file signed_gmt_file <- system.file("extdata/test.gmt", package="BioQC") signed_gmt <- readSignedGmt(signed_gmt_file) esetSignedWmwRes <- wmwTest(eset, signed_gmt, valType="p.greater") esetMat <- exprs(eset); rownames(esetMat) <- fData(eset)$GeneSymbol esetSignedWmwRes2 <- wmwTest(esetMat, signed_gmt, valType="p.greater")