<?xml version="1.0" encoding="UTF-8"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>Finds RNASeq Source Tissues Using In Situ Hybridisation Data</dc:title>
  <dc:title>R package cellOrigins version 0.1.3</dc:title>
  <dc:description>Finds the most likely originating tissue(s) and developmental stage(s) of tissue-specific RNA sequencing data. The package identifies both pure transcriptomes and mixtures of transcriptomes. The most likely identity is found through comparisons of the sequencing data with high-throughput in situ hybridisation patterns. Typical uses are the identification of cancer cell origins, validation of cell culture strain identities, validation of single-cell transcriptomes, and validation of identity and purity of flow-sorting and dissection sequencing products.</dc:description>
  <dc:type>Software</dc:type>
  <dc:relation>Imports: iterpc</dc:relation>
  <dc:creator>David Molnar &lt;dmolnar100@icloud.com&gt;</dc:creator>
  <dc:publisher>Comprehensive R Archive Network (CRAN)</dc:publisher>
  <dc:contributor>David Molnar</dc:contributor>
  <dc:rights>CC BY-NC-SA 4.0</dc:rights>
  <dc:date>2020-06-05</dc:date>
  <dc:format>application/tgz</dc:format>
  <dc:identifier>https://CRAN.R-project.org/package=cellOrigins</dc:identifier>
  <dc:identifier>doi:10.32614/CRAN.package.cellOrigins</dc:identifier>
</oai_dc:dc>
