bibentry(bibtype = "Manual",
         title = "RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.",
         author = c(person("Tomasz", "Stokowy")),
         journal = "Bioinformatics",
         year = "2016",
         url = "https://www.ncbi.nlm.nih.gov/pubmed/27288501")
