Hi, I'm interested in analyzing average density of reads from CLIP-seq experiments in the 3'UTR and around TES (transcription end site) of genes. For ChIP-seq analysis, the promoters function of "GenomicFeatures" package computes a GRanges object that spans the promoter region around the transcription start site for the transcripts in a TxDb object.Subsequent upstream 0and downstream arguments define the number of bases upstream and downstream from the transcription start site that make up the promoter region. How to create a GRanges object that spans region around TES (transcription end site) of the genes? Thank you, Marco
Thank you so much for your quick reply! I tried creating a GRanges object with a list of hg19 TES ( +/- x base pairs upstream/downstream of TES position). Is it a good solution?