Sequencing Course
Master viral genomics from sample to report. This Sequencing Course covers NGS vs Sanger, RNA extraction, primer design, alignment, variant calling, and data interpretation so biological science professionals can generate reliable, actionable results.

flexible workload from 4 to 360h
valid certificate in your country
What will I learn?
This Sequencing Course gives you practical skills to plan and execute viral sequencing projects from start to finish. Learn NGS and Sanger fundamentals, sample collection, RNA extraction, and cDNA preparation, then move into primer design, alignment, variant calling, and functional interpretation. You also master data quality control, database use, and clear, publication-ready reporting of sequence results.
Elevify advantages
Develop skills
- Viral sequencing workflows: run Sanger and NGS platforms with confidence.
- Sample-to-cDNA prep: collect swabs, extract RNA, and generate high-quality cDNA.
- Primer design essentials: create, test, and optimize viral gene primers fast.
- Variant analysis basics: align reads, call mutations, and interpret protein impact.
- Reporting genomics data: present results, limits, and clinical relevance clearly.
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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