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  "Title": "Robust Copy Number Alteration Detection (RCNA)",
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  "Authors@R": "person(\"Matt\", \"Bradley\", email = \"mbradley@emmes.com\", role = c(\"aut\", \"cre\"))",
  "Description": "Detects copy number alteration events in targeted exon\nsequencing data for tumor samples without matched normal\ncontrols. The advantage of this method is that it can be\napplied to smaller sequencing panels including evaluations of\nexon, transcript, gene, or even user specified genetic regions\nof interest. Functions in the package include steps for\nGC-content correction, calculation of quantile based normal\nkaryotype ranges, and calculation of feature score.  Cutoffs\nfor \"normal\" quantile and score are user-adjustable.",
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  "Author": "Matt Bradley [aut, cre]",
  "Maintainer": "Matt Bradley <mbradley@emmes.com>",
  "Repository": "https://cran.r-universe.dev",
  "Date/Publication": "2024-12-03 18:40:06 UTC",
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      "title": "Detecting Copy Number Variation on Targeted Exon Sequencing with RCNA",
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