build_pileup | R Documentation |
This function is used to get pileup data based on new transcript for the purpose of the downstream outlier detection analysis.
build_pileup( Pileup, caseIDs = NULL, regions, inputType = "part_intron", outputType = "part_intron" )
regions |
genomic regions formatted as chr1:1-100,200-300:+" |
inputType |
type of intronic region contained in pileup, with choices "whole_intron", "part_intron", or "only_exon"; the first is the default. |
outputType |
type of intronic region that will be included in output, with choices "whole_intron", "part_intron", or "only_exon"; the second is the default. |
regions = "chrQ:7571719-7572198,7574858-7575157,7598088-7598437:-" countPileup = build_pileup(Pileup=paste0(package_path,"SCISSOR/toydata/TOY_coverage.txt"),inputType="whole_intron",caseIDs=NULL,regions=regions)
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