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  "Type": "Package",
  "Title": "Finds RNASeq Source Tissues Using In Situ Hybridisation Data",
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  "Author": "David Molnar",
  "Maintainer": "David Molnar <dmolnar100@icloud.com>",
  "Description": "Finds the most likely originating tissue(s) and\ndevelopmental stage(s) of tissue-specific RNA sequencing data.\nThe package identifies both pure transcriptomes and mixtures of\ntranscriptomes. The most likely identity is found through\ncomparisons of the sequencing data with high-throughput in situ\nhybridisation patterns. Typical uses are the identification of\ncancer cell origins, validation of cell culture strain\nidentities, validation of single-cell transcriptomes, and\nvalidation of identity and purity of flow-sorting and\ndissection sequencing products.",
  "License": "CC BY-NC-SA 4.0",
  "Encoding": "UTF-8",
  "LazyData": "true",
  "NeedsCompilation": "no",
  "Packaged": {
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  "Repository": "https://davidhmolnar.r-universe.dev",
  "Date/Publication": "2020-06-05 08:00:02 UTC",
  "RemoteUrl": "https://github.com/cran/cellOrigins",
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