Sequencing Course
This comprehensive course equips biological professionals with vital skills in viral genomics, spanning sample processing to final reporting. Delve into NGS versus Sanger methodologies, RNA extraction techniques, primer design strategies, read alignment processes, variant detection methods, and insightful data interpretation to deliver dependable, impactful outcomes in research and clinical settings.

4 to 360 hours flexible workload
valid certificate in your country
What will I learn?
Acquire hands-on expertise to manage complete viral sequencing initiatives. Grasp core principles of NGS and Sanger sequencing, sample handling, RNA isolation, cDNA synthesis, primer development, sequence alignment, variant identification, and functional analysis. Gain proficiency in quality assurance, database navigation, and producing precise, publication-standard reports.
Elevify advantages
Develop skills
- Master viral sequencing protocols using Sanger and NGS technologies confidently.
- Perform sample-to-cDNA preparation: gather swabs, isolate RNA, synthesise superior cDNA.
- Design effective primers: develop, validate, and refine viral gene primers efficiently.
- Conduct variant analysis: align sequences, detect mutations, assess protein effects.
- Communicate genomic findings: convey results, constraints, and clinical significance lucidly.
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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