[
  {
    "title": "CNVrd2: CNVrd2: a read depth-based method to detect and genotype complex\ncommon copy number variants from next generation sequencing\ndata.",
    "author": [
      {
        "given": ["Hoang", "Tan"],
        "family": "Nguyen",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": ["Tony", "R"],
        "family": "Merriman",
        "role": {},
        "email": {},
        "comment": {}
      },
      {
        "given": "Mik",
        "family": "Black",
        "role": {},
        "email": {},
        "comment": {}
      }
    ],
    "year": "2026",
    "note": "R package version 1.50.0",
    "url": "https://bioconductor.org/packages/CNVrd2"
  }
]