Remus is a tool for identification of regulatory regions potentially associated with monogenic disease phenotypes.

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.


Example VCF [ hg19| hg38 ]

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