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Genomics Course

Genomics Course
from 4 to 360h flexible workload
valid certificate in your country

What will I learn?

This Genomics Course provides a practical, complete workflow for whole-exome sequencing in rare family disorders. Learn study design, raw data quality checks, alignment, variant calling, and joint genotyping using current best practices. Gain hands-on skills in annotation, population frequency filtering, variant prioritisation, validation, and clinical reporting, with clear examples focused on inherited cancer risks.

Elevify advantages

Develop skills

  • WES study design: plan small family exome projects for rare inherited diseases.
  • Read alignment & QC: align WES reads, check quality, and fix common issues.
  • Variant calling & filtering: run germline callers and adjust cutoffs for clean VCF files.
  • Annotation & prioritisation: use gnomAD, ClinVar, and computational scores to rank variants.
  • Clinical interpretation: classify variants using ACMG guidelines and prepare clear reports.

Suggested summary

Before starting, you can change the chapters and workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workload.
Workload: between 4 and 360 hours

What our students say

I was just promoted to Intelligence Advisor for the Prison System, and the Elevify course was crucial for me to be chosen.
EmersonPolice Investigator
The course was essential to meet the expectations of my boss and the company I work for.
SilviaNurse
Great course. A lot of valuable information.
WiltonCivil Firefighter

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