Genomics Course
Gain expertise in whole-exome sequencing for rare family disorders. Master quality checks, data alignment, variant detection, annotation, and clinical reports to turn raw genomic data into useful insights for cancer and rare disease research.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
This course provides a complete practical guide to whole-exome sequencing for rare inherited family conditions. You will cover study planning, data quality checks, alignment, variant identification, and group genotyping with top methods. Build skills in annotating variants, filtering by population frequencies, prioritising them, validating results, and preparing clinical reports, using examples from inherited cancer risks.
Elevify advantages
Develop skills
- Plan small family exome projects for rare inherited diseases.
- Align exome reads, check quality, and fix common issues.
- Run variant callers and adjust filters for accurate results.
- Use databases and scores to rank and prioritise variants.
- Apply guidelines to classify variants and write 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
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