Sequencing Course
This comprehensive course equips biological professionals with vital skills in viral genomics, spanning sample collection to final reporting. Delve into NGS and Sanger techniques, RNA extraction, primer design, read alignment, variant calling, and result interpretation to deliver precise, impactful sequencing outcomes for research and clinical applications.

4 to 360 hours of flexible workload
certificate valid in your country
What Will I Learn?
Acquire hands-on expertise to manage complete viral sequencing initiatives. Gain foundational knowledge in NGS and Sanger methods, covering sample handling, RNA isolation, cDNA synthesis, primer development, sequence alignment, variant detection, and functional analysis. Additionally, master quality assurance, database navigation, and producing professional reports for publications.
Elevify Advantages
Develop Skills
- Master viral sequencing processes using Sanger and NGS confidently.
- Perform sample-to-cDNA preparation including swab collection, RNA extraction, and quality cDNA production.
- Design, validate, and refine primers for viral genes efficiently.
- Analyse variants by aligning sequences, identifying mutations, and assessing protein effects.
- Communicate genomic findings, constraints, and clinical insights effectively in reports.
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 workload.What our students say
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