Building Skills in Genetic Interpretation

This course is designed for physicians and healthcare professionals who already have a basic understanding of genetic testing and are ready to move to the next level. If you're starting to face NGS reports in your practice and want to interpret them more confidently, this is the course for you. You'll begin with a high-level overview of the genetic data pipeline-from FASTQ to variant annotation-so you can understand how raw data becomes clinical insight.

Then, we'll dive into essential interpretation tools like ClinVar, OMIM, gnomAD, and Variant Validator, showing you how to apply them in real clinical scenarios. A major focus is placed on mastering the ACMG guidelines, with structured lectures on SNV and Indel interpretation. Through multiple real-world examples, you'll learn how to classify variants and avoid common pitfalls.

The final session brings everything together with practical test cases, helping you apply what you've learned in a hands-on way. Whether you're consulting on rare disease cases or preparing for more advanced genetic testing, this course builds a rock-solid foundation in variant interpretation. We designed it to be clear, practical, and immediately useful-so you can turn complex data into meaningful care decisions.

Let us help you level up your skills, one variant at a time.