View source: R/qsea.createSet.R
| createQseaSet | R Documentation | 
This method prepares the qseaSet object, and prepares genome wide bins. Coverage and normalization parameters are added in succeeding functions.
createQseaSet(sampleTable,BSgenome, chr.select,Regions, window_size=250 )
| BSgenome | name of BSgenome package | 
| Regions | GRanges object. If specified, only selected regions are processed | 
| chr.select | If specified, only selected chromosomes are processed | 
| sampleTable | data.frame, containing at least 3 columns: the sample names (sample_name), paths to alignment or coverage file in sam/bam/wiggle/bigwig format (file_name), and one or more test condition(s) (group). Optionally it may contain a column with alignment or coverage files for CNV analysis, and further information in the samples that are of interest for the analysis. | 
| window_size | size for the genome wide bins in base pairs | 
An object of class qseaSet, containing the sample and genome information.
Mathias Lienhard
library("BSgenome.Hsapiens.UCSC.hg19")
bam_hESCs_1 = system.file("extdata", "hESCs.MeDIP.Rep1.chr22.bam", 
    package="MEDIPSData")
bam_hESCs_2 = system.file("extdata", "hESCs.MeDIP.Rep2.chr22.bam", 
    package="MEDIPSData")
samplesTable=data.frame(sample_name=paste0("hESCs_", 1:2), 
file_name=c(bam_hESCs_1,bam_hESCs_2), 
group=rep("hESC",2),stringsAsFactors=FALSE)
qs=createQseaSet(samplesTable, BSgenome="BSgenome.Hsapiens.UCSC.hg19", 
    chr.select="chr22", window_size=500)
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