Loading Video...
NTHRYS
Arrow

Population Variation — gnomAD 1000G & Ethnopharmacology Training | Allele Frequencies, Ancestry & PGx Risk

NTHRYS >> Services >> Academic Services >> Training Programs >> Bioinformatics Training >> Pharmacogenomics, Pharmacometrics & Precision Therapeutics >> Population Variation — gnomAD 1000G & Ethnopharmacology Training | Allele Frequencies, Ancestry & PGx Risk

Population Variation — gnomAD 1000G & Ethnopharmacology — Hands-on

Learn how population genetics and allele frequency resources like gnomAD and 1000 Genomes inform pharmacogenomic interpretation. You will connect ancestry linked PGx risks, population specific variant distributions and ethnopharmacology perspectives to build fair, context aware PGx summaries.

Population Variation — gnomAD 1000G and Ethnopharmacology
Help Desk · WhatsApp
Session 1
Fee: Rs 8800
Population Genetics & Frequency Databases
  • Population genetics concepts for PGx practice
  • allele and genotype frequencies Hardy Weinberg intuition population structure overview
  • Role of frequency databases in PGx interpretation
  • distinguishing common vs rare variants linking frequency to prior probability avoid over interpretation of rare alleles
  • Overview of major germline frequency resources
  • gnomAD (conceptual use) 1000 Genomes Project regional and ancestry specific panels
Session 2
Fee: Rs 11800
gnomAD, 1000G & PGx Variant Profiles
  • Exploring gnomAD style allele frequency tables
  • global vs sub population frequencies confidence intervals and counts caveats for under represented groups
  • 1000 Genomes ancestry panels and PGx markers
  • continental ancestry groupings example PGx loci profiles linking to local populations conceptually
  • Visualizing PGx allele frequency differences
  • simple bar and heatmap style views high vs low frequency risk alleles implications for screening yield
Session 3
Fee: Rs 14800
Ethnopharmacology & Population PGx Risk
  • Ethnopharmacology concepts and equity lens
  • ancestry vs self identified ethnicity access and representation gaps ethical communication of risk
  • Case examples of population linked PGx risk
  • high frequency HLA risk alleles in regions PGx variants common in some groups impact on screening strategies
  • Balancing individual and population level information
  • avoid stereotyping care use genotype where available transparent uncertainty statements
Session 4
Fee: Rs 18800
Mini Capstone: Population Aware PGx Summary
  • Select one PGx locus and build a frequency profile
  • extract multi population frequencies identify high risk groups conceptually note data gaps and limitations
  • Summarize implications for screening and dosing policy
  • where pre emptive testing is impactful points for local guideline committees equity and consent notes
  • Deliverables: one page population PGx brief and slides
  • PDF or PPTX visual charts or tables template for future projects


PDF