# OnCo record variant-calling (term). Data CC BY-NC 4.0, attribute "Data from OnCo (onco.cc)". Whole corpus: https://onco.cc/api/v1/onco.nt
@prefix schema: <https://schema.org/> .
@prefix onco: <https://onco.cc/ns#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

<https://onco.cc/terms/variant-calling/>
  a schema:DefinedTerm ;
  onco:kind "term" ;
  schema:identifier "variant-calling" ;
  schema:name "Variant calling"@en ;
  schema:alternateName "variant calling"@en, "somatic variant calling"@en, "variant caller"@en, "variant callers"@en, "SNV calling"@en, "mutation calling"@en ;
  schema:description "Variant calling is the computational step that turns raw sequencing reads into a list of the DNA changes present in a tumour."@en ;
  schema:url <https://onco.cc/terms/variant-calling/> ;
  schema:dateModified "2026-09-24"^^xsd:date ;
  schema:sameAs <https://en.wikipedia.org/wiki/SNV_calling_from_NGS_data> ;
  schema:citation <https://doi.org/10.1038/nature12213>, <https://en.wikipedia.org/wiki/SNV_calling_from_NGS_data> ;
  onco:tag "cansim-terms" ;
  onco:related <https://onco.cc/terms/cancer-ai-vocabulary/> ;
  onco:technologies <https://onco.cc/technologies/wes-wgs/>, <https://onco.cc/technologies/ngs-bioinformatics-software/> ;
  onco:terms <https://onco.cc/terms/germline-vs-somatic/>, <https://onco.cc/terms/variant-effect-prediction/>, <https://onco.cc/terms/mutsig/> .