Sequencing Course
Acquire comprehensive skills in viral genomics, spanning sample processing to final reporting. This course explores distinctions between NGS and Sanger techniques, RNA extraction processes, primer development, alignment procedures, variant identification, and result interpretation, empowering bioscience experts to deliver dependable and practical outcomes in sequencing endeavors.

from 4 to 360h flexible workload
valid certificate in your country
What will I learn?
Gain hands-on expertise in managing complete viral sequencing initiatives. Master core principles of NGS and Sanger methods, sample gathering, RNA isolation, cDNA synthesis, primer creation, sequence alignment, variant detection, and meaningful analysis. Develop proficiency in ensuring data integrity, leveraging databases, and producing precise, report-ready sequence findings.
Elevify advantages
Develop skills
- Master viral sequencing processes: confidently operate Sanger and NGS systems.
- Excel in sample-to-cDNA preparation: handle swab collection, RNA extraction, and superior cDNA production.
- Grasp primer design fundamentals: swiftly develop, evaluate, and refine primers for viral genes.
- Learn core variant analysis: perform read alignment, mutation detection, and protein effect evaluation.
- Skillfully report genomic findings: clearly convey results, constraints, and clinical significance.
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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