OGRE-package | R Documentation |
OGRE calculates overlap between user defined annotated genomic region datasets. Any regions can be supplied such as public annotations (genes), genetic variation (SNPs, mutations), regulatory elements (TFBS, promoters, CpG islands) and basically all types of NGS output from sequencing experiments. After overlap calculation, key numbers help analyse the extend of overlaps which can also be visualized at a genomic level.
The main functions are:
OGREDataSetFromDir
- build an OGRE dataset from a user
defined directory with GRanges annotation files.
loadAnnotations
- Load dataset files containing genomic
regions annotation information from hard drive
OGREDataSet
- build an empty OGRE dataset to flexibly add
datasets from other sources like AnnotationHub or custom GRanges objects.
addDataSetFromHub
- adds datasets from AnnotationHub
addGRanges
- adds user defined GenomicRanges datasets
fOverlaps
- Finds all overlaps between query and subject
datasets
sumPlot
- calculates key numbers, tables and plots
gvizPlot
- generates a genomic plot around query elements with
overlapping subject hits.
For additional information, see the package vignette, by typing
vignette("OGRE")
. Software-related questions or issues can be posted
to the Bioconductor Support Site:
https://support.bioconductor.org
or on github:
https://https://github.com/svenbioinf/OGRE
Sven Berres, Jörg Gromoll, Marius Wöste, Sarah Sandmann, Sandra Laurentino
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