OGRE: calculate, visualize, and analyze overlap between genomic input regions and public annotations.
Sven BerresJörg GromollMarius WösteSarah SandmannSandra LaurentinoPublished in: BMC bioinformatics (2023)
OGRE's functions and built-in annotations can be applied as a downstream overlap association step, which is compatible with most genomic sequencing outputs, and can thus enrich pre-existing analyses pipelines. Compared to similar tools, OGRE shows competitive performance, offers additional features, and has been successfully applied to two recent studies. Overall, OGRE addresses the lack of tools for automatic analysis, local genomic overlap calculation, and visualization by providing an easy to use, end-to-end solution for both biologists and computational scientists.