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Multi-Omics Tumor Boards — Data to Decision | Evidence Synthesis & Clinical Reporting

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Clinical & Translational Bioinformatics / Precision Medicine >> Multi-Omics Tumor Boards — Data to Decision | Evidence Synthesis & Clinical Reporting

Multi-Omics Tumor Boards — Data to Decision — Hands-on

Learn to operate multidisciplinary tumor boards that convert complex multi-omics findings into clear, clinician-ready decisions. You will practice case intake and triage, harmonize evidence across somatic/germline, RNA signatures, proteomics and imaging, present options using recognized actionability frameworks, and produce audit-ready reports integrated with clinical workflows.

Multi-Omics Tumor Boards — Data to Decision
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Session 1
Fee: Rs 19520
Case Intake & Triage
  • Referral, consent & clinical context
  • indication & prior lines EHR abstractions privacy & governance
  • Data readiness checks
  • somatic/germline QC RNA signatures/fusions proteomics/imaging summaries
  • Triage & prioritization
  • urgency/complexity scores eligibility pre-screen agenda building
Session 2
Fee: Rs 23720
Evidence Synthesis & Actionability
  • Integrating multi-omics signals
  • WES/WGS + RNA + proteome TMB/MSI/fusions/signatures radiology & pathology bridges
  • Tiers & frameworks
  • AMP/ASCO/CAP ESCAT (ESMO) OncoKB/CIViC signals
  • Therapy & trial pathways
  • label/on-label/tissue-agnostic resistance/co-occurrence eligibility rules (high-level)
Session 3
Fee: Rs 27920
Board Simulation: Presentation & Deliberation
  • Case brief & deck building
  • one-slide summary evidence tables decision trees
  • Live presentation & Q&A
  • clinician-friendly language risk/benefit framing uncertainty & caveats
  • Consensus & minutes
  • votes & dissent action items follow-up plan
Session 4
Fee: Rs 33520
Reporting, Follow-up & Governance
  • Clinician-ready reports
  • tiers/evidence statements limitations & disclaimers patient letters (overview)
  • EHR/FHIR & CDS integration
  • FHIR Genomics profiles CDS hooks & audit trails outcome tracking
  • Governance, QA & SOPs
  • minutes & versioning re-review cadence privacy & escalation


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