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Pharmacogenomics Foundations — Genes, Drugs & Traits Training | Core PGx Concepts & Clinical Context

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Pharmacogenomics, Pharmacometrics & Precision Therapeutics >> Pharmacogenomics Foundations — Genes, Drugs & Traits Training | Core PGx Concepts & Clinical Context

Pharmacogenomics Foundations — Genes, Drugs & Traits — Hands-on

Build a strong foundation in pharmacogenomics by connecting genes, drugs and traits. Understand how variation in key pharmacogenes influences efficacy, toxicity and dosing, and learn the basic interpretation patterns that underpin guideline-driven personalized therapy.

Pharmacogenomics Foundations — Genes, Drugs & Traits
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Session 1
Fee: Rs 8800
Genetic & Clinical Foundations of PGx
  • Core genetics for pharmacogenomics
  • DNA variation & polymorphisms SNPs, indels, haplotypes inheritance patterns
  • Genes, drugs and therapeutic traits
  • PK vs PD mechanisms ADME overview efficacy vs toxicity
  • Clinical PGx use-cases and workflows
  • pre-emptive vs reactive testing PGx in hospitals stakeholders & roles
Session 2
Fee: Rs 11800
Pharmacogenes, Variants & Alleles
  • Key pharmacogene families and functions
  • CYP metabolic enzymes transporters (ABCB1, SLCO) drug targets & receptors
  • Star-alleles and phenotype categories
  • allele nomenclature activity scores poor / IM / EM / UM
  • Genotyping technologies and reports
  • arrays / qPCR NGS panels basic QC concepts
Session 3
Fee: Rs 14800
From Genotype to Drug Response
  • Basic PGx guideline interpretation patterns
  • CPIC style tables (concept) strength of evidence actionable vs informative
  • Linking phenotype to dose and drug choice
  • dose reduction / avoidance alternative agents monitoring suggestions
  • Communicating PGx findings to clinicians
  • simple risk language flags & alerts avoiding over-interpretation
Session 4
Fee: Rs 18800
Mini Capstone: PGx Case & Report
  • Case-based PGx interpretation workflow
  • select gene–drug pair derive phenotype outline recommendations
  • Structuring a basic PGx clinical summary
  • indication & context genotype & phenotype recommendations & caveats
  • Deliverables: slide deck and one-page PGx note
  • PDF/PowerPoint structured template for future clinics


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