Remus is a tool for identification of regulatory regions potentially associated with
monogenic disease
phenotypes.
Description:
Starting from a small set of genes implicated in the disease pathogenesis, Remus finds regulatory features
linked with these genes in chosen tissue-specific genome-scale regulatory datasets.
Customizable search and step-by-step process allows for iterative building of a tissue-specific set of
regions that likely play a role in regulating expression of the input genes in the tissues affected by the
disease.
Learn more...