getPromoterRegionsAllGenes,FootprintFinder-method | R Documentation |
Using the gtf table inside the genome database specified by the FootprintFinder object, return the promoter regions for every protein-coding gene in the database.
## S4 method for signature 'FootprintFinder' getPromoterRegionsAllGenes( obj, size.upstream = 10000, size.downstream = 10000, use_gene_ids = TRUE )
obj |
An object of class FootprintFinder |
size.upstream |
An integer denoting the distance upstream of each gene's transcription start site to include in the promoter region (default = 1000) |
size.downstream |
An integer denoting the distance downstream of each gene's transcription start site to include in the promoter region (default = 1000) |
use_gene_ids |
A binary indicating whether to return gene IDs or gene names (default = T) |
A GRanges object containing the promoter regions for all genes
Other FootprintFinder methods:
FootprintFinder-class
,
closeDatabaseConnections,FootprintFinder-method
,
getChromLoc,FootprintFinder-method
,
getFootprintsForGene,FootprintFinder-method
,
getFootprintsInRegion,FootprintFinder-method
,
getGenePromoterRegion,FootprintFinder-method
,
getGtfGeneBioTypes,FootprintFinder-method
,
getGtfMoleculeTypes,FootprintFinder-method
db.address <- system.file(package="trena", "extdata") genome.db.uri <- paste("sqlite:/",db.address,"mef2c.neighborhood.hg38.gtfAnnotation.db", sep = "/") project.db.uri <- paste("sqlite:/",db.address,"mef2c.neigborhood.hg38.footprints.db", sep = "/") fp <- FootprintFinder(genome.db.uri, project.db.uri) footprints <- getPromoterRegionsAllGenes(fp)
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