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  "Title": "R/Bioconductor Variant Simulator with HGVS Notation",
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  "Description": "Simulates all possible single nucleotide variants (SNVs)\nacross MANE Select transcripts including coding sequence (CDS),\nuntranslated regions (UTRs), and canonical splice sites.\nOutputs variants in HGVS notation. Provides a comprehensive\nHGVS toolkit: parsing, syntactic and semantic validation,\nnormalization (3' shifting, common affix trimming), format\nconversion (HGVS <-> VCF <-> SPDI), transcription mapping\n(genomic <-> coding), translation to protein consequence,\nbacktranslation from protein to coding variants, variant\nextraction from sequence alignment, and liftover between genome\nassemblies.",
  "License": "MIT + file LICENSE",
  "URL": "https://github.com/liu-sun/rvarsim",
  "BugReports": "https://github.com/liu-sun/rvarsim/issues",
  "Encoding": "UTF-8",
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  "Date/Publication": "2026-06-10 07:08:19 UTC",
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  "Maintainer": "Liu Sun <sunliu@yxnu.edu.cn>",
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    "transcription",
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    "normalization"
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      "page": "backtranslate_hgvs",
      "title": "Infer transcript variants from protein consequences",
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      ]
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    {
      "page": "extract_hgvs",
      "title": "Generate HGVS descriptions from reference and observed sequences",
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      ]
    },
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      "title": "Fetch MANE Select transcripts",
      "topics": [
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      ]
    },
    {
      "page": "format_hgvs",
      "title": "Format variants in HGVS notation",
      "topics": [
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      ]
    },
    {
      "page": "generate_variants",
      "title": "Generate all possible single nucleotide variants",
      "topics": [
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      ]
    },
    {
      "page": "get_transcript_structure",
      "title": "Extract transcript structure for variant simulation",
      "topics": [
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      ]
    },
    {
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      "title": "Convert HGVS to and from other variant formats",
      "topics": [
        "hgvs_conversion"
      ]
    },
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      "page": "hgvs_to_spdi",
      "title": "Convert HGVS to SPDI format",
      "topics": [
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      ]
    },
    {
      "page": "hgvs_to_vcf",
      "title": "Convert HGVS to VCF data.frame",
      "topics": [
        "hgvs_to_vcf"
      ]
    },
    {
      "page": "is_valid_hgvs",
      "title": "Check if an HGVS string is valid (convenience wrapper)",
      "topics": [
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    },
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      "page": "liftover_c_hgvs",
      "title": "Lift over a c. variant by converting to genomic, lifting, then converting back",
      "topics": [
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      ]
    },
    {
      "page": "liftover_hgvs",
      "title": "Map variants between aligned genomic sequences",
      "topics": [
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      "title": "Normalize HGVS variant descriptions",
      "topics": [
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      "title": "Parse HGVS variant descriptions",
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    },
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        "g_to_c",
        "transcribe_hgvs"
      ]
    },
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