Genomics Course
This course offers a hands-on workflow for whole-exome sequencing in rare family disorders, covering study design, data processing, variant analysis, and clinical reporting with a focus on inherited cancer risks.

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 check, 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 Mendelian disease.
- Read alignment & QC: align WES reads, assess quality, and fix common issues.
- Variant calling & filtering: run germline callers and adjust cutoffs for clean VCFs.
- Annotation & prioritisation: use gnomAD, ClinVar, and in silico scores to rank hits.
- Clinical interpretation: classify variants with ACMG rules and draft 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.What our students say
FAQs
Who is Elevify? How does it work?
Do the courses have certificates?
Are the courses free?
What is the course workload?
What are the courses like?
How do the courses work?
What is the duration of the courses?
What is the cost or price of the courses?
What is an EAD or online course and how does it work?
PDF Course