Sequencing Course
This course equips you with comprehensive skills in viral genomics, from sample collection through RNA extraction, primer design, NGS and Sanger sequencing, alignment, variant calling, to clear reporting. Ideal for biology pros seeking reliable, impactful sequence data in research or clinical settings.

flexible workload of 4 to 360h
valid certificate in your country
What will I learn?
Gain hands-on skills to manage viral sequencing projects fully, covering NGS and Sanger basics, sample handling, RNA extraction, cDNA synthesis, primer design, sequence alignment, variant detection, and result interpretation. Master quality checks, database tools, and professional reporting for publishable outcomes.
Elevify advantages
Develop skills
- Master viral sequencing workflows using Sanger and NGS confidently.
- Handle sample-to-cDNA processes: collect, extract RNA, produce quality cDNA.
- Design, test, and optimise viral primers efficiently.
- Perform variant analysis: align sequences, detect mutations, assess protein effects.
- Report genomic findings clearly with limitations and relevance.
Suggested summary
Before starting, you can change the chapters and the workload. Choose which chapter to start with. Add or remove chapters. Increase or decrease the course workloadWhat our students say
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