Learn a practical CNV workflow for NGS data—from paired-end preparation and ExomeDepth calling to structured review and interpretation.

Learn how copy-number variants can be investigated in NGS data. The course begins with core CNV concepts and detection approaches, then guides you through data preparation, calling, review, and interpretation.
The material is organized into four focused stages, with course datasets and a supplementary session available in the curriculum for continued practice.
Quizzes open once you are enrolled in the course.
No reviews yet. Be the first to review this course!

Experienced instructor in bioinformatics and computational biology.