Sequencing Course
Acquire comprehensive skills in viral genomics, spanning sample processing to final reporting. This course explores NGS alongside Sanger methods, RNA extraction techniques, primer development, read alignment, variant detection, and result interpretation, empowering bioscience experts to deliver trustworthy, practical outcomes for real-world applications.

from 4 to 360h flexible workload
certificate valid in your country
What will I learn?
Gain hands-on expertise in managing complete viral sequencing initiatives. Master core principles of NGS and Sanger sequencing, sample gathering, RNA isolation, cDNA synthesis, primer creation, sequence alignment, variant identification, and functional 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, validate, and refine primers for viral genes.
- Command variant analysis essentials: perform read alignment, mutation detection, and protein effect evaluation.
- Expertly 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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