[
  {
    "title": "RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.",
    "author": [
      {
        "given": "Tomasz",
        "family": "Stokowy",
        "role": {},
        "email": {},
        "comment": {}
      }
    ],
    "journal": "Bioinformatics",
    "year": "2016",
    "url": "https://www.ncbi.nlm.nih.gov/pubmed/27288501"
  }
]