An R program capable of intersecting a .GFF file with a chosen flanking region and large files containg genomic co-ordinates from multiple experiments and visualising the intersections genome wide as well as producing individual region plots and quantification of the intersections.
R programming language
The program also relies on a numer of R libraries, although install proceedures are included you can check before and install manually.
library(shiny)
library(ggrepel)
library(gplots)
library(RColorBrewer)
library(GenomicRanges)
library(DT)
library(ggplot2)
library(ggbio)
library(shiny)
shiny::runGitHub('GFF_Intersector','PriceJon')
Currently only GFF files are accepted along with another file containing at least chromsome, start, stop and a unique ID columns contained within the first 10 columns.
Instructions are available whilst using the program.
This is an active development and new features will be added:
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Quantification of bases intersected in the upstream/downstream/genic/IG regions.
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The ability to separate different experiment based on their ID and analyse spearately
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The ability to download high quality PDFs