Stokowy T (2016). RareVariantVis: new tool for visualization of causative variants in rare monogenic disorders using whole genome sequencing data.. https://www.ncbi.nlm.nih.gov/pubmed/27288501.

Corresponding BibTeX entry:

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