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Duration 21 hours
Course Outline
Introduction
- Overview of genetic sequencing methodologies
- Foundational understanding of genetic sequencing and testing protocols
Genetic Sequencing
- Diverse genetic sequencing approaches
- Mechanisms and application of polymerase chain reaction
- Sequencing by synthesis techniques
- Sanger sequencing principles
- Identification, classification, and reporting of variants
Clinical Genetic Testing
- Categorization of genetic testing modalities
- Traditional cytogenetic analysis
- Biochemical genetic testing methods
- Diagnostic genetic testing procedures
- Microarray diagnostic applications
- Reproductive genetic testing frameworks
Genetic Testing and Analysis
- DNA Methylation assessment
- Management of non-coding variants
- Strategies for enhancing variant classification accuracy
- Analyzing complex trait variants
- Evaluation of complex trait risk factors
- Long-read and single-cell sequencing technologies
- Advancements in personalized patient healthcare
Summary and Next Steps
Requirements
- Familiarity with foundational principles of Biology, Chemistry, and Physics
- Basic understanding of genetic fundamentals
Target Audience
- Healthcare professionals
- Healthcare workers
Testimonials (1)
The Trainer was able to adapt to our ad-hoc questions really fast.
