Hi everyone,

I would like to share an online course focused on CNV and structural variant visualization in IGV using short-read NGS data - https://www.udemy.com/course/reading-structural-variants-in-igv-short-read-ngs/?referralCode=329A93865E96ACB13973

The course covers topics such as:

read depth discordant read pairs split reads soft-clipped reads allele balance (BAF) real clinical examples

The goal was to create a practical resource for structural variant visualization and interpretation for those working with short-read NGS data.

This is not a bioinformatics course. It focuses on using IGV to visualize and recognize key patterns of structural variants, including CNVs, inversions, translocations, insertions, and retrocopies. Follow the link: https://www.udemy.com/course/reading-structural-variants-in-igv-short-read-ngs/?referralCode=329A93865E96ACB13973

There's also a concise illustrated guide on Gumroad for quick reference: https://larkass.gumroad.com/l/qvvczb