Emedgene
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Illumina Connected Software
  • Get Started with Emedgene
    • Get started with Emedgene
    • How can Emedgene help you solve a case?
  • Emedgene Analyze manual
    • Getting around the platformchevron-right
    • Managing data storagechevron-right
    • Launching analysischevron-right
    • Supported variant callerschevron-right
    • Tertiary analysis pipelinechevron-right
      • Supported reference genome assemblies
      • Joint calling in Emedgene
      • Transcript prioritization logic
      • Emedgene annotations and update frequency
      • Variant effect and severity calculation
      • Integrating variant annotations from multiple sources
      • Processing multi-nucleotide variants
    • Reviewing a casechevron-right
    • Reviewing a variantchevron-right
    • Variant visualizationchevron-right
    • Analyze Networkchevron-right
    • Settingschevron-right
    • Integrationschevron-right
    • Troubleshootingchevron-right
  • Emedgene Curate manual
    • Curatechevron-right
    • Curate Variantschevron-right
    • Curate Geneschevron-right
    • Import Curate annotations to the casechevron-right
  • Integrationschevron-right
  • Frequently Asked Questions
    • All FAQchevron-right
  • Release Notes
    • Workbench & Pipeline Updateschevron-right
    • Knowledge base updateschevron-right
    • Change logchevron-right
  • Legal
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  1. Emedgene Analyze manual

Tertiary analysis pipeline

Supported reference genome assemblieschevron-rightJoint calling in Emedgenechevron-rightTranscript prioritization logicchevron-rightEmedgene annotations and update frequencychevron-rightVariant effect and severity calculationchevron-rightIntegrating variant annotations from multiple sourceschevron-rightProcessing multi-nucleotide variantschevron-right
PreviousFormatting DRAGEN MANTA VCFs for Emedgenechevron-leftNextSupported reference genome assemblieschevron-right

Last updated 20 days ago

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