collectionGsea {HTSanalyzeR} | R Documentation

## Compute observed and permutation-based enrichment scores for a collection (list) of gene sets

### Description

This function computes observed and permutation-based scores associated with a gene set enrichment analysis for a collection of gene sets.

### Usage

    collectionGsea(collectionOfGeneSets, geneList, exponent=1, nPermutations=
    1000, minGeneSetSize=15, verbose=TRUE)

### Arguments

`collectionOfGeneSets` | a list of gene sets. Each gene set in the list is a character vector of gene identifiers.
`geneList` | a numeric or integer vector which has been named and ordered. It cannot contain any duplicates nor NAs.
`exponent` | a single numeric or integer value (set as 1 by default) specifying the exponent of the GSEA method.
`nPermutations` | a single numeric or integer value specifying the number of permutation tests for each gene set
`minGeneSetSize` | a single numeric or integer value specifying the minimum size required for a gene set to be considered.
`verbose` | a single logical value specifying to display detailed messages (when verbose=TRUE) or not (when verbose=FALSE)

### Value

`Observed.scores` | The observed scores for the given gene sets (a named vector)
`Permutation.scores` | The scores for the permutation tests (one column for each permutation and a row for each gene set)

### Author(s)

Camille Terfve, Xin Wang

### References

Subramanian, A., Tamayo, P., Mootha, V. K., Mukherjee, S., Ebert, B. L., Gillette, M. A., Paulovich, A., Pomeroy, S. L., Golub, T. R., Lander, E. S. & Mesirov, J. P. (2005) Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles. Proc. Natl. Acad. Sci. USA 102, 15545-15550.

### See Also

`FDRcollectionGsea`

### Examples

    ##example 1
    gl <- runif(100, min=0, max=5)
    gl <- gl[order(gl, decreasing=TRUE)]
    names(gl) <- as.character(sample(x=seq(from=1, to=100, by=1), size=100,
    replace=FALSE))
    gs1 <- sample(names(gl), size=20, replace=FALSE)
    gs2 <- sample(names(gl), size=20, replace=FALSE)
    gsc <- list(subset1=gs1, subset2=gs2)
    GSCscores <- collectionGsea(collectionOfGeneSets=gsc, geneList=gl,
    exponent=1, nPermutations=1000, minGeneSetSize=5)
    GSCpvalues <- permutationPvalueCollectionGsea(permScores=
    GSCscores$Permutation.scores, dataScores=GSCscores$Observed.scores)
    ##example 2
    ## Not run:
    library(org.Dm.eg.db)
    library(KEGG.db)
    ##load phenotype vector (see the vignette for details about the
    ##preprocessing of this data set)
    data("KcViab_Data4Enrich")
    DM_KEGG <- KeggGeneSets(species="Dm")
    GSCscores <- collectionGsea(collectionOfGeneSets=DM_KEGG, geneList=
    KcViab_Data4Enrich, exponent=1, nPermutations=1000, minGeneSetSize=100)
    GSCpvalues <- permutationPvalueCollectionGsea(permScores=
    GSCscores$Permutation.scores, dataScores=GSCscores$Observed.scores)

    ## End(Not run)

[Package HTSanalyzeR version 2.38.0 Index]