Emedgene
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Illumina Connected Software
Emedgene
  • Get Started with Emedgene
    • Get started with Emedgene
    • How can Emedgene help you solve a case?
  • Emedgene Analyze manual
    • Getting around the platform
    • Managing data storage
    • Launching analysis
    • Supported variant callers
    • Tertiary analysis pipeline
      • 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
      • Annotations from organization databases
    • Reviewing a case
    • Reviewing a variant
    • Variant visualization
    • Analyze Network
    • Settings
    • Integrations
    • Troubleshooting
  • Emedgene Curate manual
    • Curate
    • Curate Variants
    • Curate Genes
    • Import Curate annotations to the case
  • Integrations
  • Frequently Asked Questions
    • All FAQ
  • Release Notes
    • Workbench & Pipeline Updates
    • Knowledge base updates
    • Change log
  • 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-rightAnnotations from organization databaseschevron-right
PreviousFormatting DRAGEN MANTA VCFs for Emedgenechevron-leftNextSupported reference genome assemblieschevron-right

Last updated 1 month ago

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